rs878853113

Orientation

minus

Stabilized

minus

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

Make rs878853113(C;C)

Make rs878853113(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

15239545

Gene

PMP22

is a	snp
is	mentioned by
dbSNP	rs878853113
dbSNP (classic)	rs878853113
ClinGen	rs878853113
ebi	rs878853113
HLI	rs878853113
Exac	rs878853113
Gnomad	rs878853113
Varsome	rs878853113
LitVar	rs878853113
Map	rs878853113
PheGenI	rs878853113
Biobank	rs878853113
1000 genomes	rs878853113
hgdp	rs878853113
ensembl	rs878853113
geneview	rs878853113
scholar	rs878853113
google	rs878853113
pharmgkb	rs878853113
gwascentral	rs878853113
openSNP	rs878853113
23andMe	rs878853113
SNPshot	rs878853113
SNPdbe	rs878853113
MSV3d	rs878853113
GWAS Ctlg	rs878853113

Max Magnitude

0

ClinVar
Risk	rs878853113(C;C)
Alt	rs878853113(C;C)
Reference	Rs878853113(T;T)
Significance	Other
Disease	not provided
Variation	info
Gene	PMP22
CLNDBN	not provided
Reversed	1
HGVS	NC_000017.10:g.15142862A>G
CLNSRC
CLNACC	RCV000224582.1,