rs1057518437

Orientation

plus

Stabilized

plus

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

Make rs1057518437(A;A)

Make rs1057518437(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

149378166

Gene

TAB2

is a	snp
is	mentioned by
dbSNP	rs1057518437
dbSNP (classic)	rs1057518437
ClinGen	rs1057518437
ebi	rs1057518437
HLI	rs1057518437
Exac	rs1057518437
Gnomad	rs1057518437
Varsome	rs1057518437
LitVar	rs1057518437
Map	rs1057518437
PheGenI	rs1057518437
Biobank	rs1057518437
1000 genomes	rs1057518437
hgdp	rs1057518437
ensembl	rs1057518437
geneview	rs1057518437
scholar	rs1057518437
google	rs1057518437
pharmgkb	rs1057518437
gwascentral	rs1057518437
openSNP	rs1057518437
23andMe	rs1057518437
SNPshot	rs1057518437
SNPdbe	rs1057518437
MSV3d	rs1057518437
GWAS Ctlg	rs1057518437

Max Magnitude

0

ClinVar
Risk	rs1057518437(A;A)
Alt	rs1057518437(A;A)
Reference	Rs1057518437(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	TAB2
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.149699302C>A
CLNSRC
CLNACC	RCV000413051.1,