rs587776691

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(AG;AG)	0	common in clinvar
(AGT;AGT)	0	common in clinvar
(CT;CT)	0	common in clinvar

Make rs587776691(-;-)

Make rs587776691(-;CT)

Reference

GRCh38 38.1/142

Chromosome

17

Position

15260708

Gene

PMP22

is a	snp
is	mentioned by
dbSNP	rs587776691
dbSNP (classic)	rs587776691
ClinGen	rs587776691
ebi	rs587776691
HLI	rs587776691
Exac	rs587776691
Gnomad	rs587776691
Varsome	rs587776691
LitVar	rs587776691
Map	rs587776691
PheGenI	rs587776691
Biobank	rs587776691
1000 genomes	rs587776691
hgdp	rs587776691
ensembl	rs587776691
geneview	rs587776691
scholar	rs587776691
google	rs587776691
pharmgkb	rs587776691
gwascentral	rs587776691
openSNP	rs587776691
23andMe	rs587776691
SNPshot	rs587776691
SNPdbe	rs587776691
MSV3d	rs587776691
GWAS Ctlg	rs587776691

Max Magnitude

0

ClinVar
Risk	Rs587776691(CT;CT) rs587776691(-;-)
Alt	Rs587776691(CT;CT) rs587776691(-;-)
Reference	Rs587776691(AG;AG)
Significance	Pathogenic
Disease	Hereditary liability to pressure palsies
Variation	info
Gene	PMP22
CLNDBN	Hereditary liability to pressure palsies
Reversed	1
HGVS	NC_000017.10:g.15164025_15164026delCT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008950.5,