rs397514034

Orientation

plus

Stabilized

plus

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

Make rs397514034(-;-)

Make rs397514034(-;TC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112087898

Gene	SDHD, TIMM8B

is a	snp
is	mentioned by
dbSNP	rs397514034
dbSNP (classic)	rs397514034
ClinGen	rs397514034
ebi	rs397514034
HLI	rs397514034
Exac	rs397514034
Gnomad	rs397514034
Varsome	rs397514034
LitVar	rs397514034
Map	rs397514034
PheGenI	rs397514034
Biobank	rs397514034
1000 genomes	rs397514034
hgdp	rs397514034
ensembl	rs397514034
geneview	rs397514034
scholar	rs397514034
google	rs397514034
pharmgkb	rs397514034
gwascentral	rs397514034
openSNP	rs397514034
23andMe	rs397514034
SNPshot	rs397514034
SNPdbe	rs397514034
MSV3d	rs397514034
GWAS Ctlg	rs397514034

Max Magnitude

0

ClinVar
Risk	rs397514034(-;-)
Alt	rs397514034(-;-)
Reference	Rs397514034(TC;TC)
Significance	Pathogenic
Disease	Paragangliomas 1 not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	TIMM8B SDHD
CLNDBN	Paragangliomas 1 not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.111958622_111958623delTC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007317.2, RCV000486940.1, RCV000492163.1,