rs765028734

Orientation

plus

Stabilized

plus

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

Make rs765028734(-;G)

Make rs765028734(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

32081646

Gene

TNXB

is a	snp
is	mentioned by
dbSNP	rs765028734
dbSNP (classic)	rs765028734
ClinGen	rs765028734
ebi	rs765028734
HLI	rs765028734
Exac	rs765028734
Gnomad	rs765028734
Varsome	rs765028734
LitVar	rs765028734
Map	rs765028734
PheGenI	rs765028734
Biobank	rs765028734
1000 genomes	rs765028734
hgdp	rs765028734
ensembl	rs765028734
geneview	rs765028734
scholar	rs765028734
google	rs765028734
pharmgkb	rs765028734
gwascentral	rs765028734
openSNP	rs765028734
23andMe	rs765028734
SNPshot	rs765028734
SNPdbe	rs765028734
MSV3d	rs765028734
GWAS Ctlg	rs765028734

Max Magnitude

0

aka c.3762_3763dupGG, and also delG & dupG

ClinVar
Risk	rs765028734(G;G) rs765028734(GG;GG)
Alt	rs765028734(G;G) rs765028734(GG;GG)
Reference	Rs765028734(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	TNXB
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.32049423_32049424insGG
CLNSRC
CLNACC	RCV000487708.1,