rs137852222

Orientation

minus

Stabilized

minus

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

Make rs137852222(G;G)

Make rs137852222(G;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

77841311

Gene

MAGT1

is a	snp
is	mentioned by
dbSNP	rs137852222
dbSNP (classic)	rs137852222
ClinGen	rs137852222
ebi	rs137852222
HLI	rs137852222
Exac	rs137852222
Gnomad	rs137852222
Varsome	rs137852222
LitVar	rs137852222
Map	rs137852222
PheGenI	rs137852222
Biobank	rs137852222
1000 genomes	rs137852222
hgdp	rs137852222
ensembl	rs137852222
geneview	rs137852222
scholar	rs137852222
google	rs137852222
pharmgkb	rs137852222
gwascentral	rs137852222
openSNP	rs137852222
23andMe	rs137852222
SNPshot	rs137852222
SNPdbe	rs137852222
MSV3d	rs137852222
GWAS Ctlg	rs137852222

Max Magnitude

0

OMIM	300715
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137852222(G;G)
Alt	rs137852222(G;G)
Reference	Rs137852222(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	MAGT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000023.10:g.77096808A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000088658.2,