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rs587777013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777013(A;G)
Make rs587777013(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position59153251
GeneFAM111A
is asnp
is mentioned by
dbSNPrs587777013
ebirs587777013
HLIrs587777013
Exacrs587777013
Varsomers587777013
Maprs587777013
PheGenIrs587777013
hapmaprs587777013
1000 genomesrs587777013
hgdprs587777013
ensemblrs587777013
gopubmedrs587777013
geneviewrs587777013
scholarrs587777013
googlers587777013
pharmgkbrs587777013
gwascentralrs587777013
openSNPrs587777013
23andMers587777013
23andMe allrs587777013
SNP Nexus

SNPshotrs587777013
SNPdbers587777013
MSV3drs587777013
GWAS Ctlgrs587777013
Max Magnitude0
ClinVar
Risk rs587777013(G,T;G,T)
Alt rs587777013(G,T;G,T)
Reference rs587777013(A;A)
Significance Other
Disease Gracile bone dysplasia
Variation info
Gene FAM111A
CLNDBN Gracile bone dysplasia
Reversed 0
HGVS NC_000011.9:g.58920724A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000050212.3,