rs981049067

Orientation

plus

Stabilized

plus

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

Make rs981049067(C;C)

Make rs981049067(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

161356822

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs981049067
dbSNP (classic)	rs981049067
ClinGen	rs981049067
ebi	rs981049067
HLI	rs981049067
Exac	rs981049067
Gnomad	rs981049067
Varsome	rs981049067
LitVar	rs981049067
Map	rs981049067
PheGenI	rs981049067
Biobank	rs981049067
1000 genomes	rs981049067
hgdp	rs981049067
ensembl	rs981049067
geneview	rs981049067
scholar	rs981049067
google	rs981049067
pharmgkb	rs981049067
gwascentral	rs981049067
openSNP	rs981049067
23andMe	rs981049067
SNPshot	rs981049067
SNPdbe	rs981049067
MSV3d	rs981049067
GWAS Ctlg	rs981049067

Max Magnitude

0

ClinVar
Risk	rs981049067(A;A) rs981049067(C;C)
Alt	rs981049067(A;A) rs981049067(C;C)
Reference	Rs981049067(G;G)
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.161326612G>A; NC_000001.10:g.161326612G>C
CLNSRC
CLNACC	RCV000492239.1, RCV000477028.1,