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rs587777581

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777581(C;C)
Make rs587777581(C;T)
ReferenceGRCh38 38.1/142
Chromosome4
Position80286385
GeneFGF5
is asnp
is mentioned by
dbSNPrs587777581
ebirs587777581
HLIrs587777581
Exacrs587777581
Varsomers587777581
Maprs587777581
PheGenIrs587777581
hapmaprs587777581
1000 genomesrs587777581
hgdprs587777581
ensemblrs587777581
gopubmedrs587777581
geneviewrs587777581
scholarrs587777581
googlers587777581
pharmgkbrs587777581
gwascentralrs587777581
openSNPrs587777581
23andMers587777581
23andMe allrs587777581
SNP Nexus

SNPshotrs587777581
SNPdbers587777581
MSV3drs587777581
GWAS Ctlgrs587777581
Max Magnitude0
ClinVar
Risk rs587777581(C,G;C,G)
Alt rs587777581(C,G;C,G)
Reference rs587777581(T;T)
Significance Pathogenic
Disease Trichomegaly
Variation info
Gene FGF5
CLNDBN Trichomegaly
Reversed 0
HGVS NC_000004.11:g.81207539T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000129919.2,