rs786205594

Orientation

minus

Stabilized

minus

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

Make rs786205594(G;T)

Make rs786205594(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

118933137

Gene

TNFRSF11B

is a	snp
is	mentioned by
dbSNP	rs786205594
dbSNP (classic)	rs786205594
ClinGen	rs786205594
ebi	rs786205594
HLI	rs786205594
Exac	rs786205594
Gnomad	rs786205594
Varsome	rs786205594
LitVar	rs786205594
Map	rs786205594
PheGenI	rs786205594
Biobank	rs786205594
1000 genomes	rs786205594
hgdp	rs786205594
ensembl	rs786205594
geneview	rs786205594
scholar	rs786205594
google	rs786205594
pharmgkb	rs786205594
gwascentral	rs786205594
openSNP	rs786205594
23andMe	rs786205594
SNPshot	rs786205594
SNPdbe	rs786205594
MSV3d	rs786205594
GWAS Ctlg	rs786205594

Max Magnitude

0

ClinVar
Risk	rs786205594(T;T)
Alt	rs786205594(T;T)
Reference	Rs786205594(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNFRSF11B
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.119945376C>A
CLNSRC
CLNACC	RCV000171419.1,