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rs587777234

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777234(G;G)
Make rs587777234(G;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position12293956
GeneEDN1
is asnp
is mentioned by
dbSNPrs587777234
ebirs587777234
HLIrs587777234
Exacrs587777234
Varsomers587777234
Maprs587777234
PheGenIrs587777234
hapmaprs587777234
1000 genomesrs587777234
hgdprs587777234
ensemblrs587777234
gopubmedrs587777234
geneviewrs587777234
scholarrs587777234
googlers587777234
pharmgkbrs587777234
gwascentralrs587777234
openSNPrs587777234
23andMers587777234
23andMe allrs587777234
SNP Nexus

SNPshotrs587777234
SNPdbers587777234
MSV3drs587777234
GWAS Ctlgrs587777234
Max Magnitude0
ClinVar
Risk rs587777234(G;G)
Alt rs587777234(G;G)
Reference rs587777234(T;T)
Significance Pathogenic
Disease Question mark ears
Variation info
Gene EDN1
CLNDBN Question mark ears, isolated
Reversed 0
HGVS NC_000006.11:g.12294189T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106315.3,