rs137853277

Orientation

minus

Stabilized

minus

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

Make rs137853277(C;T)

Make rs137853277(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

171636382

Gene

MYOC

is a	snp
is	mentioned by
dbSNP	rs137853277
dbSNP (classic)	rs137853277
ClinGen	rs137853277
ebi	rs137853277
HLI	rs137853277
Exac	rs137853277
Gnomad	rs137853277
Varsome	rs137853277
LitVar	rs137853277
Map	rs137853277
PheGenI	rs137853277
Biobank	rs137853277
1000 genomes	rs137853277
hgdp	rs137853277
ensembl	rs137853277
geneview	rs137853277
scholar	rs137853277
google	rs137853277
pharmgkb	rs137853277
gwascentral	rs137853277
openSNP	rs137853277
23andMe	rs137853277
SNPshot	rs137853277
SNPdbe	rs137853277
MSV3d	rs137853277
GWAS Ctlg	rs137853277

GMAF

0.0009183

Max Magnitude

0

ClinVar
Risk	rs137853277(T;T)
Alt	rs137853277(T;T)
Reference	Rs137853277(C;C)
Significance	Untested
Disease
Variation	info
Gene	MYOC
CLNDBN	OMIM
Reversed	1
HGVS	NC_000001.10:g.171605522G>A
CLNSRC
CLNACC

OMIM	601652
Desc
Variant
Related	also