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rs587777237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587777237(A;G)
Make rs587777237(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position59125976
GeneFAM111B
is asnp
is mentioned by
dbSNPrs587777237
ebirs587777237
HLIrs587777237
Exacrs587777237
Varsomers587777237
Maprs587777237
PheGenIrs587777237
hapmaprs587777237
1000 genomesrs587777237
hgdprs587777237
ensemblrs587777237
gopubmedrs587777237
geneviewrs587777237
scholarrs587777237
googlers587777237
pharmgkbrs587777237
gwascentralrs587777237
openSNPrs587777237
23andMers587777237
23andMe allrs587777237
SNP Nexus

SNPshotrs587777237
SNPdbers587777237
MSV3drs587777237
GWAS Ctlgrs587777237
Max Magnitude0
ClinVar
Risk rs587777237(G;G)
Alt rs587777237(G;G)
Reference rs587777237(A;A)
Significance Pathogenic
Disease Poikiloderma
Variation info
Gene FAM111B
CLNDBN Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis
Reversed 0
HGVS NC_000011.9:g.58893449A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106318.2,