rs775019409

Orientation

plus

Stabilized

plus

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

Make rs775019409(G;T)

Make rs775019409(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

15230953

Gene

PMP22

is a	snp
is	mentioned by
dbSNP	rs775019409
dbSNP (classic)	rs775019409
ClinGen	rs775019409
ebi	rs775019409
HLI	rs775019409
Exac	rs775019409
Gnomad	rs775019409
Varsome	rs775019409
LitVar	rs775019409
Map	rs775019409
PheGenI	rs775019409
Biobank	rs775019409
1000 genomes	rs775019409
hgdp	rs775019409
ensembl	rs775019409
geneview	rs775019409
scholar	rs775019409
google	rs775019409
pharmgkb	rs775019409
gwascentral	rs775019409
openSNP	rs775019409
23andMe	rs775019409
SNPshot	rs775019409
SNPdbe	rs775019409
MSV3d	rs775019409
GWAS Ctlg	rs775019409

Max Magnitude

0

ClinVar
Risk	rs775019409(A;A) rs775019409(T;T)
Alt	rs775019409(A;A) rs775019409(T;T)
Reference	Rs775019409(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PMP22
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.15134270G>T
CLNSRC
CLNACC	RCV000213954.2,