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rs587777050

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777050(C;T)
Make rs587777050(T;T)
ReferenceGRCh38 38.1/142
ChromosomeX
Position77456433
GeneFGF16
is asnp
is mentioned by
dbSNPrs587777050
ebirs587777050
HLIrs587777050
Exacrs587777050
Varsomers587777050
Maprs587777050
PheGenIrs587777050
hapmaprs587777050
1000 genomesrs587777050
hgdprs587777050
ensemblrs587777050
gopubmedrs587777050
geneviewrs587777050
scholarrs587777050
googlers587777050
pharmgkbrs587777050
gwascentralrs587777050
openSNPrs587777050
23andMers587777050
23andMe allrs587777050
SNP Nexus

SNPshotrs587777050
SNPdbers587777050
MSV3drs587777050
GWAS Ctlgrs587777050
Max Magnitude0
ClinVar
Risk rs587777050(T;T)
Alt rs587777050(T;T)
Reference rs587777050(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.76711924C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000056296.6,