rs879253954

Orientation

minus

Stabilized

minus

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

Make rs879253954(A;A)

Make rs879253954(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

17

Position

15230951

Gene

PMP22

is a	snp
is	mentioned by
dbSNP	rs879253954
dbSNP (classic)	rs879253954
ClinGen	rs879253954
ebi	rs879253954
HLI	rs879253954
Exac	rs879253954
Gnomad	rs879253954
Varsome	rs879253954
LitVar	rs879253954
Map	rs879253954
PheGenI	rs879253954
Biobank	rs879253954
1000 genomes	rs879253954
hgdp	rs879253954
ensembl	rs879253954
geneview	rs879253954
scholar	rs879253954
google	rs879253954
pharmgkb	rs879253954
gwascentral	rs879253954
openSNP	rs879253954
23andMe	rs879253954
SNPshot	rs879253954
SNPdbe	rs879253954
MSV3d	rs879253954
GWAS Ctlg	rs879253954

Max Magnitude

0

ClinVar
Risk	rs879253954(A;A)
Alt	rs879253954(A;A)
Reference	Rs879253954(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PMP22
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.15134268C>T
CLNSRC
CLNACC	RCV000236879.2,