rs786205625

Orientation

minus

Stabilized

minus

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

Make rs786205625(-;-)

Make rs786205625(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

77283847

Gene

POMT2

is a	snp
is	mentioned by
dbSNP	rs786205625
dbSNP (classic)	rs786205625
ClinGen	rs786205625
ebi	rs786205625
HLI	rs786205625
Exac	rs786205625
Gnomad	rs786205625
Varsome	rs786205625
LitVar	rs786205625
Map	rs786205625
PheGenI	rs786205625
Biobank	rs786205625
1000 genomes	rs786205625
hgdp	rs786205625
ensembl	rs786205625
geneview	rs786205625
scholar	rs786205625
google	rs786205625
pharmgkb	rs786205625
gwascentral	rs786205625
openSNP	rs786205625
23andMe	rs786205625
SNPshot	rs786205625
SNPdbe	rs786205625
MSV3d	rs786205625
GWAS Ctlg	rs786205625

Max Magnitude

0

ClinVar
Risk	rs786205625(-;-)
Alt	rs786205625(-;-)
Reference	Rs786205625(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	POMT2
CLNDBN	not provided
Reversed	1
HGVS	NC_000014.8:g.77750190delG
CLNSRC
CLNACC	RCV000171478.1,