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rs876657688

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876657688(A;A)
Make rs876657688(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position77903339
GeneEDNRB, EDNRB-AS1
is asnp
is mentioned by
dbSNPrs876657688
ebirs876657688
HLIrs876657688
Exacrs876657688
Varsomers876657688
Maprs876657688
PheGenIrs876657688
hapmaprs876657688
1000 genomesrs876657688
hgdprs876657688
ensemblrs876657688
gopubmedrs876657688
geneviewrs876657688
scholarrs876657688
googlers876657688
pharmgkbrs876657688
gwascentralrs876657688
openSNPrs876657688
23andMers876657688
23andMe allrs876657688
SNP Nexus

SNPshotrs876657688
SNPdbers876657688
MSV3drs876657688
GWAS Ctlgrs876657688
Max Magnitude0
ClinVar
Risk rs876657688(A;A)
Alt rs876657688(A;A)
Reference rs876657688(G;G)
Significance Pathogenic
Disease Waardenburg syndrome
Variation info
Gene EDNRB LOC100505518
CLNDBN Waardenburg syndrome
Reversed 1
HGVS NC_000013.10:g.78477474C>T
CLNSRC
CLNACC RCV000221133.1,