rs1060503769

Orientation

plus

Stabilized

plus

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

Make rs1060503769(A;A)

Make rs1060503769(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

112094805

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs1060503769
dbSNP (classic)	rs1060503769
ClinGen	rs1060503769
ebi	rs1060503769
HLI	rs1060503769
Exac	rs1060503769
Gnomad	rs1060503769
Varsome	rs1060503769
LitVar	rs1060503769
Map	rs1060503769
PheGenI	rs1060503769
Biobank	rs1060503769
1000 genomes	rs1060503769
hgdp	rs1060503769
ensembl	rs1060503769
geneview	rs1060503769
scholar	rs1060503769
google	rs1060503769
pharmgkb	rs1060503769
gwascentral	rs1060503769
openSNP	rs1060503769
23andMe	rs1060503769
SNPshot	rs1060503769
SNPdbe	rs1060503769
MSV3d	rs1060503769
GWAS Ctlg	rs1060503769

Max Magnitude

0

ClinVar
Risk	rs1060503769(A;A)
Alt	rs1060503769(A;A)
Reference	Rs1060503769(G;G)
Significance	Pathogenic
Disease	Paragangliomas 1 Pheochromocytoma
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1 Pheochromocytoma
Reversed	0
HGVS	NC_000011.9:g.111965529G>A
CLNSRC
CLNACC	RCV000462080.1,