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rs876658569

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658569(-;-)
Make rs876658569(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position241513665
GeneFH
is asnp
is mentioned by
dbSNPrs876658569
ebirs876658569
HLIrs876658569
Exacrs876658569
Varsomers876658569
Maprs876658569
PheGenIrs876658569
hapmaprs876658569
1000 genomesrs876658569
hgdprs876658569
ensemblrs876658569
gopubmedrs876658569
geneviewrs876658569
scholarrs876658569
googlers876658569
pharmgkbrs876658569
gwascentralrs876658569
openSNPrs876658569
23andMers876658569
23andMe allrs876658569
SNP Nexus

SNPshotrs876658569
SNPdbers876658569
MSV3drs876658569
GWAS Ctlgrs876658569
Max Magnitude0
ClinVar
Risk rs876658569(;)
Alt rs876658569(;)
Reference rs876658569(G;G)
Significance 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.241676965delC
CLNSRC
CLNACC RCV000213630.1,