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rs587777015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777015(A;A)
Make rs587777015(A;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position59153247
GeneFAM111A
is asnp
is mentioned by
dbSNPrs587777015
ebirs587777015
HLIrs587777015
Exacrs587777015
Varsomers587777015
Maprs587777015
PheGenIrs587777015
hapmaprs587777015
1000 genomesrs587777015
hgdprs587777015
ensemblrs587777015
gopubmedrs587777015
geneviewrs587777015
scholarrs587777015
googlers587777015
pharmgkbrs587777015
gwascentralrs587777015
openSNPrs587777015
23andMers587777015
23andMe allrs587777015
SNP Nexus

SNPshotrs587777015
SNPdbers587777015
MSV3drs587777015
GWAS Ctlgrs587777015
Max Magnitude0
ClinVar
Risk rs587777015(A,G;A,G)
Alt rs587777015(A,G;A,G)
Reference rs587777015(C;C)
Significance Other
Disease Gracile bone dysplasia
Variation info
Gene FAM111A
CLNDBN Gracile bone dysplasia
Reversed 0
HGVS NC_000011.9:g.58920720C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000050214.3,