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rs863223966

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223966(A;G)
Make rs863223966(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position241504057
GeneFH
is asnp
is mentioned by
dbSNPrs863223966
ebirs863223966
HLIrs863223966
Exacrs863223966
Varsomers863223966
Maprs863223966
PheGenIrs863223966
hapmaprs863223966
1000 genomesrs863223966
hgdprs863223966
ensemblrs863223966
gopubmedrs863223966
geneviewrs863223966
scholarrs863223966
googlers863223966
pharmgkbrs863223966
gwascentralrs863223966
openSNPrs863223966
23andMers863223966
23andMe allrs863223966
SNP Nexus

SNPshotrs863223966
SNPdbers863223966
MSV3drs863223966
GWAS Ctlgrs863223966
Max Magnitude0
ClinVar
Risk rs863223966(G;G)
Alt rs863223966(G;G)
Reference rs863223966(A;A)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene FH
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000001.10:g.241667357T>C
CLNSRC
CLNACC RCV000196179.2, RCV000220270.1,