rs879253869

Orientation

minus

Stabilized

minus

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

Make rs879253869(A;A)

Make rs879253869(A;T)

Reference

GRCh38.p7 38.3/149

Chromosome

8

Position

81444935

Gene

PMP2

is a	snp
is	mentioned by
dbSNP	rs879253869
dbSNP (classic)	rs879253869
ClinGen	rs879253869
ebi	rs879253869
HLI	rs879253869
Exac	rs879253869
Gnomad	rs879253869
Varsome	rs879253869
LitVar	rs879253869
Map	rs879253869
PheGenI	rs879253869
Biobank	rs879253869
1000 genomes	rs879253869
hgdp	rs879253869
ensembl	rs879253869
geneview	rs879253869
scholar	rs879253869
google	rs879253869
pharmgkb	rs879253869
gwascentral	rs879253869
openSNP	rs879253869
23andMe	rs879253869
SNPshot	rs879253869
SNPdbe	rs879253869
MSV3d	rs879253869
GWAS Ctlg	rs879253869

Max Magnitude

0

ClinVar
Risk	rs879253869(A;A)
Alt	rs879253869(A;A)
Reference	Rs879253869(T;T)
Significance	Probable-Pathogenic
Disease	Peripheral neuropathy
Variation	info
Gene	PMP2
CLNDBN	Peripheral neuropathy
Reversed	1
HGVS	NC_000008.10:g.82357170A>T
CLNSRC
CLNACC	RCV000235076.1,