rs6890689

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(C;C)	0	common in complete genomics

Make rs6890689(A;C)

Reference

GRCh38 38.1/141

Chromosome

5

Position

137870871

Gene	LOC101928005, MYOT

is a	snp
is	mentioned by
dbSNP	rs6890689
dbSNP (classic)	rs6890689
ClinGen	rs6890689
ebi	rs6890689
HLI	rs6890689
Exac	rs6890689
Gnomad	rs6890689
Varsome	rs6890689
LitVar	rs6890689
Map	rs6890689
PheGenI	rs6890689
Biobank	rs6890689
1000 genomes	rs6890689
hgdp	rs6890689
ensembl	rs6890689
geneview	rs6890689
scholar	rs6890689
google	rs6890689
pharmgkb	rs6890689
gwascentral	rs6890689
openSNP	rs6890689
23andMe	rs6890689
SNPshot	rs6890689
SNPdbe	rs6890689
MSV3d	rs6890689
GWAS Ctlg	rs6890689

GMAF

0.01194

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

ClinVar
Risk	Rs6890689(C;C)
Alt	Rs6890689(C;C)
Reference	Rs6890689(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	MYOT LOC101928005
CLNDBN	not specified
Reversed	0
HGVS	NC_000005.9:g.137206560A>C
CLNSRC	HGMD
CLNACC	RCV000153527.3,