rs1057518422

Orientation

plus

Stabilized

plus

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

Make rs1057518422(C;T)

Make rs1057518422(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

149378954

Gene

TAB2

is a	snp
is	mentioned by
dbSNP	rs1057518422
dbSNP (classic)	rs1057518422
ClinGen	rs1057518422
ebi	rs1057518422
HLI	rs1057518422
Exac	rs1057518422
Gnomad	rs1057518422
Varsome	rs1057518422
LitVar	rs1057518422
Map	rs1057518422
PheGenI	rs1057518422
Biobank	rs1057518422
1000 genomes	rs1057518422
hgdp	rs1057518422
ensembl	rs1057518422
geneview	rs1057518422
scholar	rs1057518422
google	rs1057518422
pharmgkb	rs1057518422
gwascentral	rs1057518422
openSNP	rs1057518422
23andMe	rs1057518422
SNPshot	rs1057518422
SNPdbe	rs1057518422
MSV3d	rs1057518422
GWAS Ctlg	rs1057518422

Max Magnitude

0

ClinVar
Risk	rs1057518422(T;T)
Alt	rs1057518422(T;T)
Reference	Rs1057518422(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TAB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.149700090C>T
CLNSRC
CLNACC	RCV000412798.1,