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rs373901523

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs373901523(G;T)
Make rs373901523(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position56887932
GeneSLC12A3
is asnp
is mentioned by
dbSNPrs373901523
dbSNP (classic)rs373901523
ClinGenrs373901523
ebirs373901523
HLIrs373901523
Exacrs373901523
Gnomadrs373901523
Varsomers373901523
LitVarrs373901523
Maprs373901523
PheGenIrs373901523
Biobankrs373901523
1000 genomesrs373901523
hgdprs373901523
ensemblrs373901523
geneviewrs373901523
scholarrs373901523
googlers373901523
pharmgkbrs373901523
gwascentralrs373901523
openSNPrs373901523
23andMers373901523
23andMe allrs373901523
SNPshotrs373901523
SNPdbers373901523
MSV3drs373901523
GWAS Ctlgrs373901523
Max Magnitude0
ClinVar
Risk rs373901523(A;A) rs373901523(T;T)
Alt rs373901523(A;A) rs373901523(T;T)
Reference Rs373901523(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SLC12A3
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.56921844G>A
CLNSRC
CLNACC RCV000412838.1,