rs796052009

Orientation

minus

Stabilized

minus

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

Make rs796052009(-;GGA)

Make rs796052009(GGA;GGA)

Reference

GRCh38.p2 38.2/146

Chromosome

6

Position

49459092

Gene

MUT

is a	snp
is	mentioned by
dbSNP	rs796052009
dbSNP (classic)	rs796052009
ClinGen	rs796052009
ebi	rs796052009
HLI	rs796052009
Exac	rs796052009
Gnomad	rs796052009
Varsome	rs796052009
LitVar	rs796052009
Map	rs796052009
PheGenI	rs796052009
Biobank	rs796052009
1000 genomes	rs796052009
hgdp	rs796052009
ensembl	rs796052009
geneview	rs796052009
scholar	rs796052009
google	rs796052009
pharmgkb	rs796052009
gwascentral	rs796052009
openSNP	rs796052009
23andMe	rs796052009
SNPshot	rs796052009
SNPdbe	rs796052009
MSV3d	rs796052009
GWAS Ctlg	rs796052009

Max Magnitude

0

ClinVar
Risk	rs796052009(GGA;GGA)
Alt	rs796052009(GGA;GGA)
Reference	Rs796052009(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MUT
CLNDBN	not provided
Reversed	1
HGVS	NC_000006.11:g.49426806_49426808dupTCC
CLNSRC
CLNACC	RCV000186062.1,