rs370019023

Orientation

plus

Stabilized

plus

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

Make rs370019023(A;A)

Make rs370019023(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

4900805

Gene	CHRNE, C17orf107

is a	snp
is	mentioned by
dbSNP	rs370019023
dbSNP (classic)	rs370019023
ClinGen	rs370019023
ebi	rs370019023
HLI	rs370019023
Exac	rs370019023
Gnomad	rs370019023
Varsome	rs370019023
LitVar	rs370019023
Map	rs370019023
PheGenI	rs370019023
Biobank	rs370019023
1000 genomes	rs370019023
hgdp	rs370019023
ensembl	rs370019023
geneview	rs370019023
scholar	rs370019023
google	rs370019023
pharmgkb	rs370019023
gwascentral	rs370019023
openSNP	rs370019023
23andMe	rs370019023
SNPshot	rs370019023
SNPdbe	rs370019023
MSV3d	rs370019023
GWAS Ctlg	rs370019023

Max Magnitude

0

ClinVar
Risk	rs370019023(A;A) rs370019023(C;C)
Alt	rs370019023(A;A) rs370019023(C;C)
Reference	Rs370019023(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	C17orf107 CHRNE
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000017.10:g.4804100G>A; NC_000017.10:g.4804100G>C
CLNSRC
CLNACC	RCV000344538.1, RCV000414182.1,