rs876659130

Orientation

plus

Stabilized

plus

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

Make rs876659130(-;A)

Make rs876659130(A;A)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

112087951

Gene	SDHD, TIMM8B

is a	snp
is	mentioned by
dbSNP	rs876659130
dbSNP (classic)	rs876659130
ClinGen	rs876659130
ebi	rs876659130
HLI	rs876659130
Exac	rs876659130
Gnomad	rs876659130
Varsome	rs876659130
LitVar	rs876659130
Map	rs876659130
PheGenI	rs876659130
Biobank	rs876659130
1000 genomes	rs876659130
hgdp	rs876659130
ensembl	rs876659130
geneview	rs876659130
scholar	rs876659130
google	rs876659130
pharmgkb	rs876659130
gwascentral	rs876659130
openSNP	rs876659130
23andMe	rs876659130
SNPshot	rs876659130
SNPdbe	rs876659130
MSV3d	rs876659130
GWAS Ctlg	rs876659130

Max Magnitude

0

ClinVar
Risk	rs876659130(A;A)
Alt	rs876659130(A;A)
Reference	Rs876659130(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TIMM8B SDHD
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111958675dupA
CLNSRC
CLNACC	RCV000217241.1,