ClinVar Miner

List of variants in gene SLC12A3 reported as uncertain significance for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 77
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HGVS dbSNP
NM_000339.3(SLC12A3):c.*1000A>G rs886052168
NM_000339.3(SLC12A3):c.*102T>C rs886052159
NM_000339.3(SLC12A3):c.*1161A>G rs16963782
NM_000339.3(SLC12A3):c.*1266G>T rs886052169
NM_000339.3(SLC12A3):c.*1323G>C rs886052170
NM_000339.3(SLC12A3):c.*1532G>A rs531355050
NM_000339.3(SLC12A3):c.*1624C>T rs886052171
NM_000339.3(SLC12A3):c.*1647C>T rs115285739
NM_000339.3(SLC12A3):c.*1745T>C rs886052172
NM_000339.3(SLC12A3):c.*1896A>T rs886052173
NM_000339.3(SLC12A3):c.*2030T>C rs540004549
NM_000339.3(SLC12A3):c.*2051C>T rs569306925
NM_000339.3(SLC12A3):c.*2084G>A rs577055452
NM_000339.3(SLC12A3):c.*209T>A rs886052160
NM_000339.3(SLC12A3):c.*2133T>C rs574216318
NM_000339.3(SLC12A3):c.*2295T>C rs181993451
NM_000339.3(SLC12A3):c.*2318A>C rs886052174
NM_000339.3(SLC12A3):c.*2358T>C rs886052175
NM_000339.3(SLC12A3):c.*2378A>T rs886052176
NM_000339.3(SLC12A3):c.*2412del rs886052177
NM_000339.3(SLC12A3):c.*243C>T rs886052161
NM_000339.3(SLC12A3):c.*282T>A rs569410134
NM_000339.3(SLC12A3):c.*285T>C rs539777837
NM_000339.3(SLC12A3):c.*349G>A rs886052162
NM_000339.3(SLC12A3):c.*495G>A rs886052163
NM_000339.3(SLC12A3):c.*515_*516insA rs886052166
NM_000339.3(SLC12A3):c.*518T>A rs886052167
NM_000339.3(SLC12A3):c.*524dup rs11347677
NM_000339.3(SLC12A3):c.*576C>G rs139828223
NM_000339.3(SLC12A3):c.*735C>T rs749653890
NM_000339.3(SLC12A3):c.*752C>T rs8049491
NM_000339.3(SLC12A3):c.*836G>A rs149793899
NM_000339.3(SLC12A3):c.*960A>T rs545337733
NM_000339.3(SLC12A3):c.-5C>T rs200585631
NM_000339.3(SLC12A3):c.1125C>A (p.Thr375=) rs761193208
NM_000339.3(SLC12A3):c.1176C>A (p.Thr392=) rs117440321
NM_000339.3(SLC12A3):c.1216A>C (p.Asn406His) rs759532318
NM_000339.3(SLC12A3):c.1229C>A (p.Thr410Asn) rs886052157
NM_000339.3(SLC12A3):c.1248C>T (p.Cys416=) rs766672339
NM_000339.3(SLC12A3):c.1249G>A (p.Glu417Lys) rs368455032
NM_000339.3(SLC12A3):c.1284C>T (p.Thr428=) rs34216426
NM_000339.3(SLC12A3):c.1314C>T (p.Tyr438=) rs776210036
NM_000339.3(SLC12A3):c.1386C>T (p.Phe462=) rs142199602
NM_000339.3(SLC12A3):c.1392C>A (p.Ala464=) rs118121751
NM_000339.3(SLC12A3):c.1412C>A (p.Ala471Asp) rs201341355
NM_000339.3(SLC12A3):c.1606T>C (p.Phe536Leu) rs748650798
NM_000339.3(SLC12A3):c.1696A>T (p.Asn566Tyr) rs142414514
NM_000339.3(SLC12A3):c.1706C>T (p.Ala569Val) rs79351185
NM_000339.3(SLC12A3):c.1732G>A (p.Val578Met) rs139329616
NM_000339.3(SLC12A3):c.1774G>A (p.Ala592Thr) rs149644636
NM_000339.3(SLC12A3):c.1825+5G>A rs368509876
NM_000339.3(SLC12A3):c.1926-10C>G rs375828467
NM_000339.3(SLC12A3):c.1968G>A (p.Pro656=) rs150378634
NM_000339.3(SLC12A3):c.1980C>T (p.Asp660=) rs201519016
NM_000339.3(SLC12A3):c.2160C>T (p.Gly720=) rs147984554
NM_000339.3(SLC12A3):c.2221G>A (p.Gly741Arg) rs138977195
NM_000339.3(SLC12A3):c.2244G>A (p.Ser748=) rs150633177
NM_000339.3(SLC12A3):c.2272A>C (p.Ile758Leu) rs886052158
NM_000339.3(SLC12A3):c.2310C>T (p.Gly770=) rs375542454
NM_000339.3(SLC12A3):c.249G>T (p.Arg83=) rs76750525
NM_000339.3(SLC12A3):c.2517C>T (p.Thr839=) rs539069621
NM_000339.3(SLC12A3):c.2548G>A (p.Gly850Ser) rs769412145
NM_000339.3(SLC12A3):c.2573T>A (p.Leu858His) rs185927948
NM_000339.3(SLC12A3):c.2605A>G (p.Lys869Glu) rs200253241
NM_000339.3(SLC12A3):c.2820C>T (p.Asn940=) rs13306666
NM_000339.3(SLC12A3):c.286G>A (p.Glu96Lys) rs886052156
NM_000339.3(SLC12A3):c.2947G>A (p.Val983Ile) rs373092349
NM_000339.3(SLC12A3):c.2991G>A (p.Ser997=) rs35082264
NM_000339.3(SLC12A3):c.3014C>A (p.Thr1005Asn) rs201058248
NM_000339.3(SLC12A3):c.36C>T (p.Asp12=) rs117987946
NM_000339.3(SLC12A3):c.404G>A (p.Arg135His) rs769047841
NM_000339.3(SLC12A3):c.409G>A (p.Gly137Ser) rs143774019
NM_000339.3(SLC12A3):c.422G>C (p.Gly141Ala) rs146854174
NM_000339.3(SLC12A3):c.694G>A (p.Ala232Thr) rs201318038
NM_000339.3(SLC12A3):c.741+8C>T rs200257610
NM_000339.3(SLC12A3):c.774C>T (p.Asn258=) rs111578437
NM_000339.3(SLC12A3):c.81C>G (p.Ser27Arg) rs201850644

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