rs17856697

Orientation

plus

Stabilized

plus

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

Make rs17856697(A;G)

Make rs17856697(G;G)

Reference

GRCh38 38.1/141

Chromosome

17

Position

7445306

Gene	CHRNB1, FGF11

is a	snp
is	mentioned by
dbSNP	rs17856697
dbSNP (classic)	rs17856697
ClinGen	rs17856697
ebi	rs17856697
HLI	rs17856697
Exac	rs17856697
Gnomad	rs17856697
Varsome	rs17856697
LitVar	rs17856697
Map	rs17856697
PheGenI	rs17856697
Biobank	rs17856697
1000 genomes	rs17856697
hgdp	rs17856697
ensembl	rs17856697
geneview	rs17856697
scholar	rs17856697
google	rs17856697
pharmgkb	rs17856697
gwascentral	rs17856697
openSNP	rs17856697
23andMe	rs17856697
SNPshot	rs17856697
SNPdbe	rs17856697
MSV3d	rs17856697
GWAS Ctlg	rs17856697

GMAF

0.1713

Max Magnitude

0

[PMID 22406075] Association of single nucleotide polymorphisms of nicotinic acetylcholine receptor subunits with cervical neoplasia

ClinVar
Risk	rs17856697(G;G)
Alt	rs17856697(G;G)
Reference	Rs17856697(A;A)
Significance	Non-pathogenic
Disease	not specified Congenital Myasthenic Syndrome
Variation	info
Gene	CHRNB1 FGF11
CLNDBN	not specified Congenital Myasthenic Syndrome, Dominant/Recessive
Reversed	0
HGVS	NC_000017.10:g.7348625A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000116727.3, RCV000329220.1,