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rs1057516925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516925(A;A)
Make rs1057516925(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position34238964
GeneSLC12A6
is asnp
is mentioned by
dbSNPrs1057516925
dbSNP (old)rs1057516925
ClinGenrs1057516925
ebirs1057516925
HLIrs1057516925
Exacrs1057516925
Gnomadrs1057516925
Varsomers1057516925
Maprs1057516925
PheGenIrs1057516925
Biobankrs1057516925
1000 genomesrs1057516925
hgdprs1057516925
ensemblrs1057516925
gopubmedrs1057516925
geneviewrs1057516925
scholarrs1057516925
googlers1057516925
pharmgkbrs1057516925
gwascentralrs1057516925
openSNPrs1057516925
23andMers1057516925
23andMe allrs1057516925
SNPshotrs1057516925
SNPdbers1057516925
MSV3drs1057516925
GWAS Ctlgrs1057516925
Max Magnitude0
ClinVar
Risk rs1057516925(A;A)
Alt rs1057516925(A;A)
Reference Rs1057516925(G;G)
Significance Probable-Pathogenic
Disease Andermann syndrome
Variation info
Gene SLC12A6
CLNDBN Andermann syndrome
Reversed 1
HGVS NC_000015.9:g.34531165C>T
CLNSRC
CLNACC RCV000412124.1,