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rs786202200

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786202200(A;A)
Make rs786202200(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161328395
GeneSDHC
is asnp
is mentioned by
dbSNPrs786202200
ebirs786202200
HLIrs786202200
Exacrs786202200
Varsomers786202200
Maprs786202200
PheGenIrs786202200
hapmaprs786202200
1000 genomesrs786202200
hgdprs786202200
ensemblrs786202200
gopubmedrs786202200
geneviewrs786202200
scholarrs786202200
googlers786202200
pharmgkbrs786202200
gwascentralrs786202200
openSNPrs786202200
23andMers786202200
23andMe allrs786202200
SNP Nexus

SNPshotrs786202200
SNPdbers786202200
MSV3drs786202200
GWAS Ctlgrs786202200
Max Magnitude0
ClinVar
Risk rs786202200(A;A)
Alt rs786202200(A;A)
Reference rs786202200(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene SDHC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.161298185G>A
CLNSRC
CLNACC RCV000164903.1,