rs281865419

Orientation

plus

Stabilized

plus

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

Make rs281865419(C;T)

Make rs281865419(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

31577157

Gene

TNF

is a	snp
is	mentioned by
dbSNP	rs281865419
dbSNP (classic)	rs281865419
ClinGen	rs281865419
ebi	rs281865419
HLI	rs281865419
Exac	rs281865419
Gnomad	rs281865419
Varsome	rs281865419
LitVar	rs281865419
Map	rs281865419
PheGenI	rs281865419
Biobank	rs281865419
1000 genomes	rs281865419
hgdp	rs281865419
ensembl	rs281865419
geneview	rs281865419
scholar	rs281865419
google	rs281865419
pharmgkb	rs281865419
gwascentral	rs281865419
openSNP	rs281865419
23andMe	rs281865419
SNPshot	rs281865419
SNPdbe	rs281865419
MSV3d	rs281865419
GWAS Ctlg	rs281865419

Max Magnitude

0

ClinVar
Risk	rs281865419(T;T)
Alt	rs281865419(T;T)
Reference	Rs281865419(C;C)
Significance	Pathogenic
Disease	TNF receptor binding
Variation	info
Gene	TNF
CLNDBN	TNF receptor binding, altered
Reversed	0
HGVS	NC_000006.11:g.31544934C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013187.24,