rs876661014

Orientation

minus

Stabilized

minus

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

Make rs876661014(C;G)

Make rs876661014(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

12

Position

6333777

Gene

TNFRSF1A

is a	snp
is	mentioned by
dbSNP	rs876661014
dbSNP (classic)	rs876661014
ClinGen	rs876661014
ebi	rs876661014
HLI	rs876661014
Exac	rs876661014
Gnomad	rs876661014
Varsome	rs876661014
LitVar	rs876661014
Map	rs876661014
PheGenI	rs876661014
Biobank	rs876661014
1000 genomes	rs876661014
hgdp	rs876661014
ensembl	rs876661014
geneview	rs876661014
scholar	rs876661014
google	rs876661014
pharmgkb	rs876661014
gwascentral	rs876661014
openSNP	rs876661014
23andMe	rs876661014
SNPshot	rs876661014
SNPdbe	rs876661014
MSV3d	rs876661014
GWAS Ctlg	rs876661014

Max Magnitude

0

ClinVar
Risk	rs876661014(G;G)
Alt	rs876661014(G;G)
Reference	Rs876661014(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNFRSF1A
CLNDBN	not provided
Reversed	1
HGVS	NC_000012.11:g.6442943G>C
CLNSRC
CLNACC	RCV000218061.2,