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rs372505976

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372505976(C;C)
Make rs372505976(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241508641
GeneFH
is asnp
is mentioned by
dbSNPrs372505976
ebirs372505976
HLIrs372505976
Exacrs372505976
Varsomers372505976
Maprs372505976
PheGenIrs372505976
hapmaprs372505976
1000 genomesrs372505976
hgdprs372505976
ensemblrs372505976
gopubmedrs372505976
geneviewrs372505976
scholarrs372505976
googlers372505976
pharmgkbrs372505976
gwascentralrs372505976
openSNPrs372505976
23andMers372505976
23andMe allrs372505976
SNP Nexus

SNPshotrs372505976
SNPdbers372505976
MSV3drs372505976
GWAS Ctlgrs372505976
Max Magnitude0
ClinVar
Risk rs372505976(C;C)
Alt rs372505976(C;C)
Reference rs372505976(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FH
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000001.10:g.241671941T>C
CLNSRC
CLNACC RCV000163828.1, RCV000195694.2,