rs104894310

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6.2	Hereditary PGL/PCC Syndrome
(G;G)	0	common in clinvar

Make rs104894310(A;A)

Reference

GRCh38 38.1/141

Chromosome

11

Position

112086921

Gene	SDHD, TIMM8B

is a	snp
is	mentioned by
dbSNP	rs104894310
dbSNP (classic)	rs104894310
ClinGen	rs104894310
ebi	rs104894310
HLI	rs104894310
Exac	rs104894310
Gnomad	rs104894310
Varsome	rs104894310
LitVar	rs104894310
Map	rs104894310
PheGenI	rs104894310
Biobank	rs104894310
1000 genomes	rs104894310
hgdp	rs104894310
ensembl	rs104894310
geneview	rs104894310
scholar	rs104894310
google	rs104894310
pharmgkb	rs104894310
gwascentral	rs104894310
openSNP	rs104894310
23andMe	rs104894310
SNPshot	rs104894310
SNPdbe	rs104894310
MSV3d	rs104894310
GWAS Ctlg	rs104894310

Max Magnitude

6.2

OMIM	602690
Desc
Variant	0026
Related	also

ClinVar
Risk	rs104894310(A;A)
Alt	rs104894310(A;A)
Reference	Rs104894310(G;G)
Significance	Pathogenic
Disease	Pheochromocytoma
Variation	info
Gene	TIMM8B SDHD
CLNDBN	Pheochromocytoma
Reversed	0
HGVS	NC_000011.9:g.111957645G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007325.2,