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rs587777579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777579(-;-)
Make rs587777579(-;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position80275013
GeneFGF5
is asnp
is mentioned by
dbSNPrs587777579
dbSNP (old)rs587777579
ClinGenrs587777579
ebirs587777579
HLIrs587777579
Exacrs587777579
Gnomadrs587777579
Varsomers587777579
Maprs587777579
PheGenIrs587777579
Biobankrs587777579
1000 genomesrs587777579
hgdprs587777579
ensemblrs587777579
gopubmedrs587777579
geneviewrs587777579
scholarrs587777579
googlers587777579
pharmgkbrs587777579
gwascentralrs587777579
openSNPrs587777579
23andMers587777579
23andMe allrs587777579
SNP Nexus

SNPshotrs587777579
SNPdbers587777579
MSV3drs587777579
GWAS Ctlgrs587777579
Max Magnitude0
ClinVar
Risk rs587777579(-;-)
Alt rs587777579(-;-)
Reference Rs587777579(G;G)
Significance Pathogenic
Disease Trichomegaly
Variation info
Gene FGF5
CLNDBN Trichomegaly
Reversed 0
HGVS NC_000004.11:g.81196167delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000129916.2,