List of variants in gene SLC19A3 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_025243.4(SLC19A3):c.151-311T>A	rs13400826	0.96045
NM_025243.3(SLC19A3):c.-90C>T	rs4972919	0.61232
NM_025243.4(SLC19A3):c.979+213G>A	rs7602410	0.61040
NM_025243.4(SLC19A3):c.-2-224G>T	rs68136760	0.36655
NM_025243.4(SLC19A3):c.1314+173G>A	rs13025803	0.36290
NM_025243.4(SLC19A3):c.-2-62G>A	rs6713116	0.18515
NM_025243.4(SLC19A3):c.1049T>C (p.Val350Ala)	rs34507036	0.09001
NM_025243.4(SLC19A3):c.979+182A>G	rs112266944	0.08911
NM_025243.4(SLC19A3):c.*203C>T	rs80307329	0.07960
NM_025243.4(SLC19A3):c.1314+121C>A	rs74971746	0.07959
NM_025243.4(SLC19A3):c.1172+196A>T	rs79988924	0.04585
NM_025243.4(SLC19A3):c.980-235G>A	rs78560438	0.04581
NM_025243.4(SLC19A3):c.1172+209A>G	rs77029550	0.04578
NM_025243.4(SLC19A3):c.979+93G>A	rs80269916	0.04498
NM_025243.4(SLC19A3):c.979+42G>C	rs79612836	0.04495
NM_025243.4(SLC19A3):c.150+198A>G	rs76278804	0.04493
NM_025243.4(SLC19A3):c.1172+273A>G	rs6721696	0.04198
NM_025243.4(SLC19A3):c.1173-47C>T	rs73997321	0.04170
NM_025243.4(SLC19A3):c.150+203A>C	rs74387373	0.03958
NM_025243.4(SLC19A3):c.980-205G>A	rs75081601	0.03368
NM_025243.4(SLC19A3):c.520G>A (p.Val174Ile)	rs59736804	0.03276
NM_025243.4(SLC19A3):c.1315-123C>T	rs76072698	0.03025
NM_025243.4(SLC19A3):c.980-246G>A	rs6745885	0.02080
NM_025243.4(SLC19A3):c.42C>T (p.Tyr14=)	rs34080459	0.01664
NM_025243.4(SLC19A3):c.756G>A (p.Leu252=)	rs12185721	0.00883
NM_025243.4(SLC19A3):c.309G>A (p.Val103=)	rs142837989	0.00618
NM_025243.4(SLC19A3):c.421G>A (p.Gly141Ser)	rs148144444	0.00577
NM_025243.4(SLC19A3):c.546G>A (p.Val182=)	rs143188189	0.00263
NM_025243.4(SLC19A3):c.1132A>G (p.Ile378Val)	rs117864472	0.00062
GRCh37/hg19 2q36.3(chr2:228568652-228612016)x1
NM_025243.4(SLC19A3):c.-2-76del	rs71039629
NM_025243.4(SLC19A3):c.1172+273_1172+277del	rs140315029
NM_025243.4(SLC19A3):c.390G>T (p.Val130=)	rs376187918
NM_025243.4(SLC19A3):c.979+279_979+282del	rs113074927
NM_025243.4(SLC19A3):c.980-40dup	rs79287293
NM_025243.4(SLC19A3):c.980-4del	rs11334205

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