rs886037628

Orientation

minus

Stabilized

minus

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

Make rs886037628(-;T)

Make rs886037628(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

4899255

Gene	CHRNE, C17orf107

is a	snp
is	mentioned by
dbSNP	rs886037628
dbSNP (classic)	rs886037628
ClinGen	rs886037628
ebi	rs886037628
HLI	rs886037628
Exac	rs886037628
Gnomad	rs886037628
Varsome	rs886037628
LitVar	rs886037628
Map	rs886037628
PheGenI	rs886037628
Biobank	rs886037628
1000 genomes	rs886037628
hgdp	rs886037628
ensembl	rs886037628
geneview	rs886037628
scholar	rs886037628
google	rs886037628
pharmgkb	rs886037628
gwascentral	rs886037628
openSNP	rs886037628
23andMe	rs886037628
SNPshot	rs886037628
SNPdbe	rs886037628
MSV3d	rs886037628
GWAS Ctlg	rs886037628

Max Magnitude

0

ClinVar
Risk	rs886037628(T;T)
Alt	rs886037628(T;T)
Reference	Rs886037628(-;-)
Significance	Pathogenic
Disease	Myasthenic syndrome
Variation	info
Gene	C17orf107 CHRNE
CLNDBN	Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
Reversed	1
HGVS	NC_000017.10:g.4802550_4802551insA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000020023.30,