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

rs1057517818

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517818(C;C)
Make rs1057517818(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position161328498
GeneSDHC
is asnp
is mentioned by
dbSNPrs1057517818
dbSNP (old)rs1057517818
ClinGenrs1057517818
ebirs1057517818
HLIrs1057517818
Exacrs1057517818
Gnomadrs1057517818
Varsomers1057517818
LitVarrs1057517818
Maprs1057517818
PheGenIrs1057517818
Biobankrs1057517818
1000 genomesrs1057517818
hgdprs1057517818
ensemblrs1057517818
gopubmedrs1057517818
geneviewrs1057517818
scholarrs1057517818
googlers1057517818
pharmgkbrs1057517818
gwascentralrs1057517818
openSNPrs1057517818
23andMers1057517818
23andMe allrs1057517818
SNPshotrs1057517818
SNPdbers1057517818
MSV3drs1057517818
GWAS Ctlgrs1057517818
Max Magnitude0
ClinVar
Risk rs1057517818(C;C)
Alt rs1057517818(C;C)
Reference Rs1057517818(G;G)
Significance Probable-Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene SDHC
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000001.10:g.161298288G>C
CLNSRC
CLNACC RCV000414585.1, RCV000492312.1,