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rs587777236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587777236(G;G)
Make rs587777236(G;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position59125958
GeneFAM111B
is asnp
is mentioned by
dbSNPrs587777236
ebirs587777236
HLIrs587777236
Exacrs587777236
Varsomers587777236
Maprs587777236
PheGenIrs587777236
hapmaprs587777236
1000 genomesrs587777236
hgdprs587777236
ensemblrs587777236
gopubmedrs587777236
geneviewrs587777236
scholarrs587777236
googlers587777236
pharmgkbrs587777236
gwascentralrs587777236
openSNPrs587777236
23andMers587777236
23andMe allrs587777236
SNP Nexus

SNPshotrs587777236
SNPdbers587777236
MSV3drs587777236
GWAS Ctlgrs587777236
Max Magnitude0
ClinVar
Risk rs587777236(G;G)
Alt rs587777236(G;G)
Reference rs587777236(T;T)
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.58893431T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000106317.2,