rs1057518015

Orientation

plus

Stabilized

plus

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

Make rs1057518015(C;T)

Make rs1057518015(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

149379110

Gene

TAB2

is a	snp
is	mentioned by
dbSNP	rs1057518015
dbSNP (classic)	rs1057518015
ClinGen	rs1057518015
ebi	rs1057518015
HLI	rs1057518015
Exac	rs1057518015
Gnomad	rs1057518015
Varsome	rs1057518015
LitVar	rs1057518015
Map	rs1057518015
PheGenI	rs1057518015
Biobank	rs1057518015
1000 genomes	rs1057518015
hgdp	rs1057518015
ensembl	rs1057518015
geneview	rs1057518015
scholar	rs1057518015
google	rs1057518015
pharmgkb	rs1057518015
gwascentral	rs1057518015
openSNP	rs1057518015
23andMe	rs1057518015
SNPshot	rs1057518015
SNPdbe	rs1057518015
MSV3d	rs1057518015
GWAS Ctlg	rs1057518015

Max Magnitude

0

ClinVar
Risk	rs1057518015(T;T)
Alt	rs1057518015(T;T)
Reference	Rs1057518015(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TAB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.149700246C>T
CLNSRC
CLNACC	RCV000414624.1,