rs1057517934

Orientation

plus

Stabilized

plus

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

Make rs1057517934(C;T)

Make rs1057517934(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

149378318

Gene

TAB2

is a	snp
is	mentioned by
dbSNP	rs1057517934
dbSNP (classic)	rs1057517934
ClinGen	rs1057517934
ebi	rs1057517934
HLI	rs1057517934
Exac	rs1057517934
Gnomad	rs1057517934
Varsome	rs1057517934
LitVar	rs1057517934
Map	rs1057517934
PheGenI	rs1057517934
Biobank	rs1057517934
1000 genomes	rs1057517934
hgdp	rs1057517934
ensembl	rs1057517934
geneview	rs1057517934
scholar	rs1057517934
google	rs1057517934
pharmgkb	rs1057517934
gwascentral	rs1057517934
openSNP	rs1057517934
23andMe	rs1057517934
SNPshot	rs1057517934
SNPdbe	rs1057517934
MSV3d	rs1057517934
GWAS Ctlg	rs1057517934

Max Magnitude

0

ClinVar
Risk	rs1057517934(T;T)
Alt	rs1057517934(T;T)
Reference	Rs1057517934(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TAB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.149699454C>T
CLNSRC
CLNACC	RCV000413501.1,