rs786205147

Orientation

plus

Stabilized

plus

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

Make rs786205147(A;A)

Make rs786205147(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

161340638

Gene

SDHC

is a	snp
is	mentioned by
dbSNP	rs786205147
dbSNP (classic)	rs786205147
ClinGen	rs786205147
ebi	rs786205147
HLI	rs786205147
Exac	rs786205147
Gnomad	rs786205147
Varsome	rs786205147
LitVar	rs786205147
Map	rs786205147
PheGenI	rs786205147
Biobank	rs786205147
1000 genomes	rs786205147
hgdp	rs786205147
ensembl	rs786205147
geneview	rs786205147
scholar	rs786205147
google	rs786205147
pharmgkb	rs786205147
gwascentral	rs786205147
openSNP	rs786205147
23andMe	rs786205147
SNPshot	rs786205147
SNPdbe	rs786205147
MSV3d	rs786205147
GWAS Ctlg	rs786205147

Max Magnitude

0

ClinVar
Risk	rs786205147(A;A)
Alt	rs786205147(A;A)
Reference	Rs786205147(G;G)
Significance	Probable-Pathogenic
Disease	Carney triad
Variation	info
Gene	SDHC
CLNDBN	Carney triad
Reversed	0
HGVS	NC_000001.10:g.161310428G>A
CLNSRC	National Institutes of Health / The Eunice Kennedy Shriver National Institute of Child Health and Human Development
CLNACC	RCV000170332.1,