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rs876657660

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876657660(C;C)
Make rs876657660(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position37983384
GeneLOC105373026, POLR2F, SOX10
is asnp
is mentioned by
dbSNPrs876657660
ebirs876657660
HLIrs876657660
Exacrs876657660
Varsomers876657660
Maprs876657660
PheGenIrs876657660
hapmaprs876657660
1000 genomesrs876657660
hgdprs876657660
ensemblrs876657660
gopubmedrs876657660
geneviewrs876657660
scholarrs876657660
googlers876657660
pharmgkbrs876657660
gwascentralrs876657660
openSNPrs876657660
23andMers876657660
23andMe allrs876657660
SNP Nexus

SNPshotrs876657660
SNPdbers876657660
MSV3drs876657660
GWAS Ctlgrs876657660
Max Magnitude0
ClinVar
Risk rs876657660(C;C)
Alt rs876657660(C;C)
Reference rs876657660(T;T)
Significance Probable-Pathogenic
Disease Waardenburg syndrome
Variation info
Gene SOX10 POLR2F
CLNDBN Waardenburg syndrome
Reversed 1
HGVS NC_000022.10:g.38379391A>G
CLNSRC
CLNACC RCV000215786.1,