rs759226183

Orientation

plus

Stabilized

plus

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

Make rs759226183(A;A)

Make rs759226183(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

4900998

Gene	CHRNE, C17orf107

is a	snp
is	mentioned by
dbSNP	rs759226183
dbSNP (classic)	rs759226183
ClinGen	rs759226183
ebi	rs759226183
HLI	rs759226183
Exac	rs759226183
Gnomad	rs759226183
Varsome	rs759226183
LitVar	rs759226183
Map	rs759226183
PheGenI	rs759226183
Biobank	rs759226183
1000 genomes	rs759226183
hgdp	rs759226183
ensembl	rs759226183
geneview	rs759226183
scholar	rs759226183
google	rs759226183
pharmgkb	rs759226183
gwascentral	rs759226183
openSNP	rs759226183
23andMe	rs759226183
SNPshot	rs759226183
SNPdbe	rs759226183
MSV3d	rs759226183
GWAS Ctlg	rs759226183

Max Magnitude

0

ClinVar
Risk	rs759226183(A;A)
Alt	rs759226183(A;A)
Reference	Rs759226183(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	C17orf107 CHRNE
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.4804293G>A
CLNSRC
CLNACC	RCV000420519.1,