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rs587777014

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777014(A;G)
Make rs587777014(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position59152680
GeneFAM111A
is asnp
is mentioned by
dbSNPrs587777014
ebirs587777014
HLIrs587777014
Exacrs587777014
Varsomers587777014
Maprs587777014
PheGenIrs587777014
hapmaprs587777014
1000 genomesrs587777014
hgdprs587777014
ensemblrs587777014
gopubmedrs587777014
geneviewrs587777014
scholarrs587777014
googlers587777014
pharmgkbrs587777014
gwascentralrs587777014
openSNPrs587777014
23andMers587777014
23andMe allrs587777014
SNP Nexus

SNPshotrs587777014
SNPdbers587777014
MSV3drs587777014
GWAS Ctlgrs587777014
Max Magnitude0
ClinVar
Risk rs587777014(G;G)
Alt rs587777014(G;G)
Reference rs587777014(A;A)
Significance Other
Disease Gracile bone dysplasia
Variation info
Gene FAM111A
CLNDBN Gracile bone dysplasia
Reversed 0
HGVS NC_000011.9:g.58920153A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000050213.3,