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rs587780262

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780262(-;-)
Make rs587780262(-;G)
Make rs587780262(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position83462592
GeneFAM175A
is asnp
is mentioned by
dbSNPrs587780262
ebirs587780262
HLIrs587780262
Exacrs587780262
Varsomers587780262
Maprs587780262
PheGenIrs587780262
hapmaprs587780262
1000 genomesrs587780262
hgdprs587780262
ensemblrs587780262
gopubmedrs587780262
geneviewrs587780262
scholarrs587780262
googlers587780262
pharmgkbrs587780262
gwascentralrs587780262
openSNPrs587780262
23andMers587780262
23andMe allrs587780262
SNP Nexus

SNPshotrs587780262
SNPdbers587780262
MSV3drs587780262
GWAS Ctlgrs587780262
Max Magnitude0
ClinVar
Risk rs587780262(G;G)
Alt rs587780262(G;G)
Reference rs587780262(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FAM175A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000004.11:g.84383746dupC
CLNSRC
CLNACC RCV000116184.2,