ClinVar Miner

List of variants in gene ALMS1 reported as benign for monogenic diabetes

Included ClinVar conditions (64):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_001378454.1(ALMS1):c.5786G>A (p.Arg1929Gln) rs17009061 0.02260
NM_001378454.1(ALMS1):c.4962G>T (p.Lys1654Asn) rs28730853 0.02251
NM_001378454.1(ALMS1):c.11054G>A (p.Ser3685Asn) rs11896293 0.02143
NM_001378454.1(ALMS1):c.11266G>A (p.Gly3756Ser) rs34927702 0.01962
NM_001378454.1(ALMS1):c.4154C>G (p.Thr1385Arg) rs115517108 0.01785
NM_001378454.1(ALMS1):c.671C>A (p.Pro224His) rs11889925 0.01714
NM_001378454.1(ALMS1):c.10303A>G (p.Lys3435Glu) rs34071195 0.01643
NM_001378454.1(ALMS1):c.1871A>G (p.His624Arg) rs41291187 0.01596
NM_001378454.1(ALMS1):c.5359A>G (p.Asn1787Asp) rs45608038 0.01548
NM_001378454.1(ALMS1):c.1144A>G (p.Thr382Ala) rs28730849 0.01527
NM_001378454.1(ALMS1):c.6553C>T (p.Pro2185Ser) rs77555300 0.01000
NM_001378454.1(ALMS1):c.5433G>C (p.Lys1811Asn) rs78039319 0.00994
NM_001378454.1(ALMS1):c.8835C>G (p.Asn2945Lys) rs35062203 0.00814
NM_001378454.1(ALMS1):c.10628C>G (p.Thr3543Ser) rs45501594 0.00668
NM_001378454.1(ALMS1):c.3193T>C (p.Ser1065Pro) rs28730852 0.00579
NM_001378454.1(ALMS1):c.10272G>C (p.Lys3424Asn) rs34398445 0.00566
NM_001378454.1(ALMS1):c.6752A>G (p.Asp2251Gly) rs28730855 0.00515
NM_001378454.1(ALMS1):c.11821G>A (p.Gly3941Ser) rs61741524 0.00422
NM_001378454.1(ALMS1):c.6464A>G (p.Asp2155Gly) rs58093963 0.00401
NM_001378454.1(ALMS1):c.7268A>G (p.Asn2423Ser) rs75145370 0.00401
NM_001378454.1(ALMS1):c.9886A>G (p.Thr3296Ala) rs58806616 0.00273
NM_001378454.1(ALMS1):c.9914A>G (p.Asn3305Ser) rs142022233 0.00236
NM_001378454.1(ALMS1):c.3311G>A (p.Gly1104Asp) rs201074268 0.00199
NM_001378454.1(ALMS1):c.1453A>G (p.Ile485Val) rs73945001 0.00195
NM_001378454.1(ALMS1):c.6302C>G (p.Ser2101Trp) rs28730854
NM_001378454.1(ALMS1):c.6302C>T (p.Ser2101Leu) rs28730854

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