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rs1057516898

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057516898(A;A)
Make rs1057516898(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position34257702
GeneSLC12A6
is asnp
is mentioned by
dbSNPrs1057516898
dbSNP (old)rs1057516898
ClinGenrs1057516898
ebirs1057516898
HLIrs1057516898
Exacrs1057516898
Gnomadrs1057516898
Varsomers1057516898
Maprs1057516898
PheGenIrs1057516898
Biobankrs1057516898
1000 genomesrs1057516898
hgdprs1057516898
ensemblrs1057516898
gopubmedrs1057516898
geneviewrs1057516898
scholarrs1057516898
googlers1057516898
pharmgkbrs1057516898
gwascentralrs1057516898
openSNPrs1057516898
23andMers1057516898
23andMe allrs1057516898
SNPshotrs1057516898
SNPdbers1057516898
MSV3drs1057516898
GWAS Ctlgrs1057516898
Max Magnitude0
ClinVar
Risk rs1057516898(A;A)
Alt rs1057516898(A;A)
Reference Rs1057516898(G;G)
Significance Probable-Pathogenic
Disease Andermann syndrome
Variation info
Gene SLC12A6
CLNDBN Andermann syndrome
Reversed 1
HGVS NC_000015.9:g.34549903C>T
CLNSRC
CLNACC RCV000411505.1,