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rs876660446

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660446(A;A)
Make rs876660446(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position241502559
GeneFH
is asnp
is mentioned by
dbSNPrs876660446
ebirs876660446
HLIrs876660446
Exacrs876660446
Varsomers876660446
Maprs876660446
PheGenIrs876660446
hapmaprs876660446
1000 genomesrs876660446
hgdprs876660446
ensemblrs876660446
gopubmedrs876660446
geneviewrs876660446
scholarrs876660446
googlers876660446
pharmgkbrs876660446
gwascentralrs876660446
openSNPrs876660446
23andMers876660446
23andMe allrs876660446
SNP Nexus

SNPshotrs876660446
SNPdbers876660446
MSV3drs876660446
GWAS Ctlgrs876660446
Max Magnitude0
ClinVar
Risk rs876660446(A;A)
Alt rs876660446(A;A)
Reference rs876660446(C;C)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FH
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.241665859G>T
CLNSRC
CLNACC RCV000222416.1,