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rs587777051

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777051(A;A)
Make rs587777051(A;C)
ReferenceGRCh38 38.1/142
ChromosomeX
Position77456368
GeneFGF16
is asnp
is mentioned by
dbSNPrs587777051
ebirs587777051
HLIrs587777051
Exacrs587777051
Varsomers587777051
Maprs587777051
PheGenIrs587777051
hapmaprs587777051
1000 genomesrs587777051
hgdprs587777051
ensemblrs587777051
gopubmedrs587777051
geneviewrs587777051
scholarrs587777051
googlers587777051
pharmgkbrs587777051
gwascentralrs587777051
openSNPrs587777051
23andMers587777051
23andMe allrs587777051
SNP Nexus

SNPshotrs587777051
SNPdbers587777051
MSV3drs587777051
GWAS Ctlgrs587777051
Max Magnitude0
ClinVar
Risk rs587777051(A;A)
Alt rs587777051(A;A)
Reference rs587777051(C;C)
Significance Pathogenic
Disease Metacarpal 4-5 fusion
Variation info
Gene FGF16
CLNDBN Metacarpal 4-5 fusion
Reversed 0
HGVS NC_000023.10:g.76711859C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000056297.3,