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rs587777233

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777233(A;A)
Make rs587777233(A;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position12292467
GeneEDN1
is asnp
is mentioned by
dbSNPrs587777233
ebirs587777233
HLIrs587777233
Exacrs587777233
Varsomers587777233
Maprs587777233
PheGenIrs587777233
hapmaprs587777233
1000 genomesrs587777233
hgdprs587777233
ensemblrs587777233
gopubmedrs587777233
geneviewrs587777233
scholarrs587777233
googlers587777233
pharmgkbrs587777233
gwascentralrs587777233
openSNPrs587777233
23andMers587777233
23andMe allrs587777233
SNP Nexus

SNPshotrs587777233
SNPdbers587777233
MSV3drs587777233
GWAS Ctlgrs587777233
Max Magnitude0
ClinVar
Risk rs587777233(A;A)
Alt rs587777233(A;A)
Reference rs587777233(T;T)
Significance Pathogenic
Disease Question mark ears
Variation info
Gene EDN1
CLNDBN Question mark ears, isolated
Reversed 0
HGVS NC_000006.11:g.12292700T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000106314.3,