rs1060503767

Orientation

minus

Stabilized

minus

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

Make rs1060503767(-;-)

Make rs1060503767(-;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

1

Position

17053997

Gene

SDHB

is a	snp
is	mentioned by
dbSNP	rs1060503767
dbSNP (classic)	rs1060503767
ClinGen	rs1060503767
ebi	rs1060503767
HLI	rs1060503767
Exac	rs1060503767
Gnomad	rs1060503767
Varsome	rs1060503767
LitVar	rs1060503767
Map	rs1060503767
PheGenI	rs1060503767
Biobank	rs1060503767
1000 genomes	rs1060503767
hgdp	rs1060503767
ensembl	rs1060503767
geneview	rs1060503767
scholar	rs1060503767
google	rs1060503767
pharmgkb	rs1060503767
gwascentral	rs1060503767
openSNP	rs1060503767
23andMe	rs1060503767
SNPshot	rs1060503767
SNPdbe	rs1060503767
MSV3d	rs1060503767
GWAS Ctlg	rs1060503767

Max Magnitude

0

ClinVar
Risk	rs1060503767(-;-)
Alt	rs1060503767(-;-)
Reference	Rs1060503767(TC;TC)
Significance	Pathogenic
Disease	Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Variation	info
Gene	SDHB
CLNDBN	Gastrointestinal stromal tumor Paragangliomas 4 Pheochromocytoma
Reversed	1
HGVS	NC_000001.10:g.17380492_17380493delGA
CLNSRC
CLNACC	RCV000464374.1,