rs1060503770

Orientation

plus

Stabilized

plus

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

Make rs1060503770(C;T)

Make rs1060503770(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

112094815

Gene

SDHD

is a	snp
is	mentioned by
dbSNP	rs1060503770
dbSNP (classic)	rs1060503770
ClinGen	rs1060503770
ebi	rs1060503770
HLI	rs1060503770
Exac	rs1060503770
Gnomad	rs1060503770
Varsome	rs1060503770
LitVar	rs1060503770
Map	rs1060503770
PheGenI	rs1060503770
Biobank	rs1060503770
1000 genomes	rs1060503770
hgdp	rs1060503770
ensembl	rs1060503770
geneview	rs1060503770
scholar	rs1060503770
google	rs1060503770
pharmgkb	rs1060503770
gwascentral	rs1060503770
openSNP	rs1060503770
23andMe	rs1060503770
SNPshot	rs1060503770
SNPdbe	rs1060503770
MSV3d	rs1060503770
GWAS Ctlg	rs1060503770

Max Magnitude

0

ClinVar
Risk	rs1060503770(T;T)
Alt	rs1060503770(T;T)
Reference	Rs1060503770(C;C)
Significance	Pathogenic
Disease	Paragangliomas 1 Pheochromocytoma Hereditary cancer-predisposing syndrome
Variation	info
Gene	SDHD
CLNDBN	Paragangliomas 1 Pheochromocytoma Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111965539C>T
CLNSRC
CLNACC	RCV000456537.1, RCV000492697.1,