rs1135809

Orientation

minus

Stabilized

minus

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

Make rs1135809(A;C)

Make rs1135809(C;C)

Reference

GRCh37 37.1/131

Chromosome

6

Position

32042955

Gene

TNXB

is a	snp
is	mentioned by
dbSNP	rs1135809
dbSNP (classic)	rs1135809
ClinGen	rs1135809
ebi	rs1135809
HLI	rs1135809
Exac	rs1135809
Gnomad	rs1135809
Varsome	rs1135809
LitVar	rs1135809
Map	rs1135809
PheGenI	rs1135809
Biobank	rs1135809
1000 genomes	rs1135809
hgdp	rs1135809
ensembl	rs1135809
geneview	rs1135809
scholar	rs1135809
google	rs1135809
pharmgkb	rs1135809
gwascentral	rs1135809
openSNP	rs1135809
23andMe	rs1135809
SNPshot	rs1135809
SNPdbe	rs1135809
MSV3d	rs1135809
GWAS Ctlg	rs1135809

Max Magnitude

0

ClinVar
Risk	rs1135809(C;C)
Alt	rs1135809(C;C)
Reference	Rs1135809(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	TNXB
CLNDBN	not specified
Reversed	1
HGVS	NC_000006.11:g.32010732T>G
CLNSRC
CLNACC	RCV000252128.1,