rs749890642

Orientation

plus

Stabilized

plus

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

Make rs749890642(A;A)

Make rs749890642(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

32089277

Gene

TNXB

is a	snp
is	mentioned by
dbSNP	rs749890642
dbSNP (classic)	rs749890642
ClinGen	rs749890642
ebi	rs749890642
HLI	rs749890642
Exac	rs749890642
Gnomad	rs749890642
Varsome	rs749890642
LitVar	rs749890642
Map	rs749890642
PheGenI	rs749890642
Biobank	rs749890642
1000 genomes	rs749890642
hgdp	rs749890642
ensembl	rs749890642
geneview	rs749890642
scholar	rs749890642
google	rs749890642
pharmgkb	rs749890642
gwascentral	rs749890642
openSNP	rs749890642
23andMe	rs749890642
SNPshot	rs749890642
SNPdbe	rs749890642
MSV3d	rs749890642
GWAS Ctlg	rs749890642

Max Magnitude

0

ClinVar
Risk	rs749890642(A;A)
Alt	rs749890642(A;A)
Reference	Rs749890642(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNXB
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.32057054G>A
CLNSRC
CLNACC	RCV000413590.1,