rs797044596

Merged into

rs121913648

Orientation

minus

Stabilized

minus

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

Make rs797044596(-;-)

Make rs797044596(-;AGA)

Reference

GRCh38.p2 38.2/146

Chromosome

14

Position

23416105

Gene	MHRT, MYH7

is a	snp
is	mentioned by
dbSNP	rs797044596
dbSNP (classic)	rs797044596
ClinGen	rs797044596
ebi	rs797044596
HLI	rs797044596
Exac	rs797044596
Gnomad	rs797044596
Varsome	rs797044596
LitVar	rs797044596
Map	rs797044596
PheGenI	rs797044596
Biobank	rs797044596
1000 genomes	rs797044596
hgdp	rs797044596
ensembl	rs797044596
geneview	rs797044596
scholar	rs797044596
google	rs797044596
pharmgkb	rs797044596
gwascentral	rs797044596
openSNP	rs797044596
23andMe	rs797044596
SNPshot	rs797044596
SNPdbe	rs797044596
MSV3d	rs797044596
GWAS Ctlg	rs797044596

Status

Merged into rs121913648

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs797044596(AGA;AGA)
Significance	Pathogenic
Disease	Laing distal myopathy Myopathy
Variation	info
Gene	MYH7 MHRT
CLNDBN	Laing distal myopathy Myopathy, distal, 1
Reversed	1
HGVS	NC_000014.8:g.23885314_23885316delTCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000015173.26, RCV000192202.1,