rs1057517818

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057517818(C;C)

Make rs1057517818(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

161328498

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs1057517818
dbSNP (classic)	rs1057517818
ClinGen	rs1057517818
ebi	rs1057517818
HLI	rs1057517818
Exac	rs1057517818
Gnomad	rs1057517818
Varsome	rs1057517818
LitVar	rs1057517818
Map	rs1057517818
PheGenI	rs1057517818
Biobank	rs1057517818
1000 genomes	rs1057517818
hgdp	rs1057517818
ensembl	rs1057517818
geneview	rs1057517818
scholar	rs1057517818
google	rs1057517818
pharmgkb	rs1057517818
gwascentral	rs1057517818
openSNP	rs1057517818
23andMe	rs1057517818
SNPshot	rs1057517818
SNPdbe	rs1057517818
MSV3d	rs1057517818
GWAS Ctlg	rs1057517818

Max Magnitude

0

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,