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rs587777232

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777232(A;A)
Make rs587777232(A;C)
ReferenceGRCh38 38.1/142
Chromosome6
Position12292506
GeneEDN1
is asnp
is mentioned by
dbSNPrs587777232
ebirs587777232
HLIrs587777232
Exacrs587777232
Varsomers587777232
Maprs587777232
PheGenIrs587777232
hapmaprs587777232
1000 genomesrs587777232
hgdprs587777232
ensemblrs587777232
gopubmedrs587777232
geneviewrs587777232
scholarrs587777232
googlers587777232
pharmgkbrs587777232
gwascentralrs587777232
openSNPrs587777232
23andMers587777232
23andMe allrs587777232
SNP Nexus

SNPshotrs587777232
SNPdbers587777232
MSV3drs587777232
GWAS Ctlgrs587777232
Max Magnitude0
ClinVar
Risk rs587777232(A;A)
Alt rs587777232(A;A)
Reference rs587777232(C;C)
Significance Pathogenic
Disease Auriculocondylar syndrome 3
Variation info
Gene EDN1
CLNDBN Auriculocondylar syndrome 3
Reversed 0
HGVS NC_000006.11:g.12292739C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000106313.3,