rs281865132

Orientation

minus

Stabilized

minus

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

Make rs281865132(C;T)

Make rs281865132(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161305974

Gene

MPZ

is a	snp
is	mentioned by
dbSNP	rs281865132
dbSNP (classic)	rs281865132
ClinGen	rs281865132
ebi	rs281865132
HLI	rs281865132
Exac	rs281865132
Gnomad	rs281865132
Varsome	rs281865132
LitVar	rs281865132
Map	rs281865132
PheGenI	rs281865132
Biobank	rs281865132
1000 genomes	rs281865132
hgdp	rs281865132
ensembl	rs281865132
geneview	rs281865132
scholar	rs281865132
google	rs281865132
pharmgkb	rs281865132
gwascentral	rs281865132
openSNP	rs281865132
23andMe	rs281865132
SNPshot	rs281865132
SNPdbe	rs281865132
MSV3d	rs281865132
GWAS Ctlg	rs281865132

Max Magnitude

0

ClinVar
Risk	rs281865132(T;T)
Alt	rs281865132(T;T)
Reference	Rs281865132(C;C)
Significance	Pathogenic
Disease	Charcot-Marie-Tooth disease
Variation	info
Gene	MPZ
CLNDBN	Charcot-Marie-Tooth disease, demyelinating, type 1b
Reversed	1
HGVS	NC_000001.10:g.161275764G>A
CLNSRC	ClinVar GeneReviews
CLNACC	RCV000033925.1,