rs919271118

Orientation

plus

Stabilized

plus

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

Make rs919271118(A;A)

Make rs919271118(A;G)

Make rs919271118(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

4900796

Gene	CHRNE, C17orf107

is a	snp
is	mentioned by
dbSNP	rs919271118
dbSNP (classic)	rs919271118
ClinGen	rs919271118
ebi	rs919271118
HLI	rs919271118
Exac	rs919271118
Gnomad	rs919271118
Varsome	rs919271118
LitVar	rs919271118
Map	rs919271118
PheGenI	rs919271118
Biobank	rs919271118
1000 genomes	rs919271118
hgdp	rs919271118
ensembl	rs919271118
geneview	rs919271118
scholar	rs919271118
google	rs919271118
pharmgkb	rs919271118
gwascentral	rs919271118
openSNP	rs919271118
23andMe	rs919271118
SNPshot	rs919271118
SNPdbe	rs919271118
MSV3d	rs919271118
GWAS Ctlg	rs919271118

Max Magnitude

0

ClinVar
Risk	rs919271118(A;A)
Alt	rs919271118(A;A)
Reference	Rs919271118(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	C17orf107 CHRNE
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.4804091C>T
CLNSRC
CLNACC	RCV000431016.1,