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rs137876115

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137876115(C;C)
Make rs137876115(C;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position83470315
GeneFAM175A
is asnp
is mentioned by
dbSNPrs137876115
ebirs137876115
HLIrs137876115
Exacrs137876115
Varsomers137876115
Maprs137876115
PheGenIrs137876115
hapmaprs137876115
1000 genomesrs137876115
hgdprs137876115
ensemblrs137876115
gopubmedrs137876115
geneviewrs137876115
scholarrs137876115
googlers137876115
pharmgkbrs137876115
gwascentralrs137876115
openSNPrs137876115
23andMers137876115
23andMe allrs137876115
SNP Nexus

SNPshotrs137876115
SNPdbers137876115
MSV3drs137876115
GWAS Ctlgrs137876115
Max Magnitude0
ClinVar
Risk rs137876115(A,C,T;A,C,T)
Alt rs137876115(A,C,T;A,C,T)
Reference rs137876115(G;G)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene FAM175A
CLNDBN not provided not specified
Reversed 0
HGVS NC_000004.11:g.84391468G>A; NC_000004.11:g.84391468G>C
CLNSRC ClinVar GeneDx
CLNACC RCV000116190.2, RCV000116189.2,