Have questions? Visit https://www.reddit.com/r/SNPedia

rs764575966

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs764575966(C;T)
Make rs764575966(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position161356832
GeneSDHC
is asnp
is mentioned by
dbSNPrs764575966
ebirs764575966
HLIrs764575966
Exacrs764575966
Varsomers764575966
Maprs764575966
PheGenIrs764575966
hapmaprs764575966
1000 genomesrs764575966
hgdprs764575966
ensemblrs764575966
gopubmedrs764575966
geneviewrs764575966
scholarrs764575966
googlers764575966
pharmgkbrs764575966
gwascentralrs764575966
openSNPrs764575966
23andMers764575966
23andMe allrs764575966
SNP Nexus

SNPshotrs764575966
SNPdbers764575966
MSV3drs764575966
GWAS Ctlgrs764575966
Max Magnitude0
ClinVar
Risk rs764575966(T;T)
Alt rs764575966(T;T)
Reference rs764575966(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 3
Variation info
Gene SDHC
CLNDBN Hereditary cancer-predisposing syndrome Gastrointestinal stromal tumor Paragangliomas 3
Reversed 0
HGVS NC_000001.10:g.161326622C>T
CLNSRC
CLNACC RCV000162467.1, RCV000232178.1,