rs281865128

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	6.1	Charcot-Marie-Tooth Disease, type 1
(G;G)	0	common in clinvar

Make rs281865128(C;C)

Make rs281865128(C;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

161306426

Gene

MPZ

is a	snp
is	mentioned by
dbSNP	rs281865128
dbSNP (classic)	rs281865128
ClinGen	rs281865128
ebi	rs281865128
HLI	rs281865128
Exac	rs281865128
Gnomad	rs281865128
Varsome	rs281865128
LitVar	rs281865128
Map	rs281865128
PheGenI	rs281865128
Biobank	rs281865128
1000 genomes	rs281865128
hgdp	rs281865128
ensembl	rs281865128
geneview	rs281865128
scholar	rs281865128
google	rs281865128
pharmgkb	rs281865128
gwascentral	rs281865128
openSNP	rs281865128
23andMe	rs281865128
SNPshot	rs281865128
SNPdbe	rs281865128
MSV3d	rs281865128
GWAS Ctlg	rs281865128

Max Magnitude

6.1

ClinVar
Risk	rs281865128(A;A) rs281865128(C;C)
Alt	rs281865128(A;A) rs281865128(C;C)
Reference	Rs281865128(G;G)
Significance	Other
Disease	Charcot-Marie-Tooth disease Charcot-Marie-Tooth disease not provided
Variation	info
Gene	MPZ
CLNDBN	Charcot-Marie-Tooth disease, demyelinating, type 1b Charcot-Marie-Tooth disease, type I not provided
Reversed	1
HGVS	NC_000001.10:g.161276216C>G; NC_000001.10:g.161276216C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000033919.3, RCV000205003.3, RCV000217802.1, RCV000193606.1,