rs587776653

Orientation

plus

Stabilized

plus

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

Make rs587776653(G;T)

Make rs587776653(T;T)

Reference

GRCh38 38.1/142

Chromosome

1

Position

161356841

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs587776653
dbSNP (classic)	rs587776653
ClinGen	rs587776653
ebi	rs587776653
HLI	rs587776653
Exac	rs587776653
Gnomad	rs587776653
Varsome	rs587776653
LitVar	rs587776653
Map	rs587776653
PheGenI	rs587776653
Biobank	rs587776653
1000 genomes	rs587776653
hgdp	rs587776653
ensembl	rs587776653
geneview	rs587776653
scholar	rs587776653
google	rs587776653
pharmgkb	rs587776653
gwascentral	rs587776653
openSNP	rs587776653
23andMe	rs587776653
SNPshot	rs587776653
SNPdbe	rs587776653
MSV3d	rs587776653
GWAS Ctlg	rs587776653

Max Magnitude

0

ClinVar
Risk	rs587776653(A;A) rs587776653(T;T)
Alt	rs587776653(A;A) rs587776653(T;T)
Reference	Rs587776653(G;G)
Significance	Pathogenic
Disease	Paraganglioma and gastric stromal sarcoma Gastrointestinal stromal tumor Carney triad Hereditary cancer-predisposing syndrome Paragangliomas 3
Variation	info
Gene	SDHC
CLNDBN	Paraganglioma and gastric stromal sarcoma Gastrointestinal stromal tumor Carney triad Hereditary cancer-predisposing syndrome Paragangliomas 3
Reversed	0
HGVS	NC_000001.10:g.161326631G>A; NC_000001.10:g.161326631G>C; NC_000001.10:g.161326631G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007666.4, RCV000023194.3, RCV000170333.1, RCV000492714.1, RCV000007664.3,