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rs587780261

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587780261(-;-)
Make rs587780261(-;T)
Make rs587780261(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position83462666
GeneFAM175A
is asnp
is mentioned by
dbSNPrs587780261
ebirs587780261
HLIrs587780261
Exacrs587780261
Varsomers587780261
Maprs587780261
PheGenIrs587780261
hapmaprs587780261
1000 genomesrs587780261
hgdprs587780261
ensemblrs587780261
gopubmedrs587780261
geneviewrs587780261
scholarrs587780261
googlers587780261
pharmgkbrs587780261
gwascentralrs587780261
openSNPrs587780261
23andMers587780261
23andMe allrs587780261
SNP Nexus

SNPshotrs587780261
SNPdbers587780261
MSV3drs587780261
GWAS Ctlgrs587780261
Max Magnitude0
ClinVar
Risk rs587780261(T;T)
Alt rs587780261(T;T)
Reference rs587780261(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene FAM175A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000004.11:g.84383820dupA
CLNSRC
CLNACC RCV000116183.2,