rs879255562

Orientation

minus

Stabilized

minus

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

Make rs879255562(-;-)

Make rs879255562(-;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

4899529

Gene	CHRNE, C17orf107

is a	snp
is	mentioned by
dbSNP	rs879255562
dbSNP (classic)	rs879255562
ClinGen	rs879255562
ebi	rs879255562
HLI	rs879255562
Exac	rs879255562
Gnomad	rs879255562
Varsome	rs879255562
LitVar	rs879255562
Map	rs879255562
PheGenI	rs879255562
Biobank	rs879255562
1000 genomes	rs879255562
hgdp	rs879255562
ensembl	rs879255562
geneview	rs879255562
scholar	rs879255562
google	rs879255562
pharmgkb	rs879255562
gwascentral	rs879255562
openSNP	rs879255562
23andMe	rs879255562
SNPshot	rs879255562
SNPdbe	rs879255562
MSV3d	rs879255562
GWAS Ctlg	rs879255562

Max Magnitude

0

ClinVar
Risk	rs879255562(-;-)
Alt	rs879255562(-;-)
Reference	Rs879255562(T;T)
Significance	Pathogenic
Disease	Myasthenic syndrome not provided
Variation	info
Gene	C17orf107 CHRNE
CLNDBN	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency not provided
Reversed	1
HGVS	NC_000017.10:g.4802824delA
CLNSRC	CHRNE homepage - Leiden Muscular Dystrophy pages OMIM Allelic Variant
CLNACC	RCV000020016.29, RCV000326857.1,