rs876658301

Orientation

plus

Stabilized

plus

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

Make rs876658301(-;T)

Make rs876658301(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

161356811

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs876658301
dbSNP (classic)	rs876658301
ClinGen	rs876658301
ebi	rs876658301
HLI	rs876658301
Exac	rs876658301
Gnomad	rs876658301
Varsome	rs876658301
LitVar	rs876658301
Map	rs876658301
PheGenI	rs876658301
Biobank	rs876658301
1000 genomes	rs876658301
hgdp	rs876658301
ensembl	rs876658301
geneview	rs876658301
scholar	rs876658301
google	rs876658301
pharmgkb	rs876658301
gwascentral	rs876658301
openSNP	rs876658301
23andMe	rs876658301
SNPshot	rs876658301
SNPdbe	rs876658301
MSV3d	rs876658301
GWAS Ctlg	rs876658301

Max Magnitude

0

ClinVar
Risk	rs876658301(T;T)
Alt	rs876658301(T;T)
Reference	Rs876658301(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHC
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000001.10:g.161326601dupT
CLNSRC
CLNACC	RCV000215996.1,