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rs200796606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs200796606(G;G)
Make rs200796606(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position241502552
GeneFH
is asnp
is mentioned by
dbSNPrs200796606
ebirs200796606
HLIrs200796606
Exacrs200796606
Varsomers200796606
Maprs200796606
PheGenIrs200796606
hapmaprs200796606
1000 genomesrs200796606
hgdprs200796606
ensemblrs200796606
gopubmedrs200796606
geneviewrs200796606
scholarrs200796606
googlers200796606
pharmgkbrs200796606
gwascentralrs200796606
openSNPrs200796606
23andMers200796606
23andMe allrs200796606
SNP Nexus

SNPshotrs200796606
SNPdbers200796606
MSV3drs200796606
GWAS Ctlgrs200796606
Max Magnitude0
ClinVar
Risk rs200796606(G;G)
Alt rs200796606(G;G)
Reference rs200796606(T;T)
Significance Other
Disease Fumarase deficiency Hereditary cancer-predisposing syndrome not provided
Variation info
Gene FH
CLNDBN Fumarase deficiency Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000001.10:g.241665852T>G
CLNSRC ClinVar GeneReviews University of Washington
CLNACC RCV000034920.3, RCV000163798.1, RCV000199873.1,