rs777219451

Orientation

plus

Stabilized

plus

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

Make rs777219451(C;T)

Make rs777219451(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

232540617

Gene

CHRNG

is a	snp
is	mentioned by
dbSNP	rs777219451
dbSNP (classic)	rs777219451
ClinGen	rs777219451
ebi	rs777219451
HLI	rs777219451
Exac	rs777219451
Gnomad	rs777219451
Varsome	rs777219451
LitVar	rs777219451
Map	rs777219451
PheGenI	rs777219451
Biobank	rs777219451
1000 genomes	rs777219451
hgdp	rs777219451
ensembl	rs777219451
geneview	rs777219451
scholar	rs777219451
google	rs777219451
pharmgkb	rs777219451
gwascentral	rs777219451
openSNP	rs777219451
23andMe	rs777219451
SNPshot	rs777219451
SNPdbe	rs777219451
MSV3d	rs777219451
GWAS Ctlg	rs777219451

Max Magnitude

0

ClinVar
Risk	rs777219451(T;T)
Alt	rs777219451(T;T)
Reference	Rs777219451(C;C)
Significance	Probable-Pathogenic
Disease	Peripheral neuropathy
Variation	info
Gene	CHRNG
CLNDBN	Peripheral neuropathy
Reversed	0
HGVS	NC_000002.11:g.233405327C>T
CLNSRC
CLNACC	RCV000449634.1,