rs1057519570

Orientation

plus

Stabilized

plus

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

Make rs1057519570(-;-)

Make rs1057519570(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

68174095

Gene

MYPN

is a	snp
is	mentioned by
dbSNP	rs1057519570
dbSNP (classic)	rs1057519570
ClinGen	rs1057519570
ebi	rs1057519570
HLI	rs1057519570
Exac	rs1057519570
Gnomad	rs1057519570
Varsome	rs1057519570
LitVar	rs1057519570
Map	rs1057519570
PheGenI	rs1057519570
Biobank	rs1057519570
1000 genomes	rs1057519570
hgdp	rs1057519570
ensembl	rs1057519570
geneview	rs1057519570
scholar	rs1057519570
google	rs1057519570
pharmgkb	rs1057519570
gwascentral	rs1057519570
openSNP	rs1057519570
23andMe	rs1057519570
SNPshot	rs1057519570
SNPdbe	rs1057519570
MSV3d	rs1057519570
GWAS Ctlg	rs1057519570

Max Magnitude

0

ClinVar
Risk	rs1057519570(-;-)
Alt	rs1057519570(-;-)
Reference	Rs1057519570(A;A)
Significance	Pathogenic
Disease	Nemaline myopathy 11
Variation	info
Gene	MYPN
CLNDBN	Nemaline myopathy 11, autosomal recessive
Reversed	0
HGVS	NC_000010.10:g.69933852delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000417052.1,