rs387906347

Orientation

minus

Stabilized

minus

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

Make rs387906347(A;A)

Make rs387906347(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

36219856

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs387906347
dbSNP (classic)	rs387906347
ClinGen	rs387906347
ebi	rs387906347
HLI	rs387906347
Exac	rs387906347
Gnomad	rs387906347
Varsome	rs387906347
LitVar	rs387906347
Map	rs387906347
PheGenI	rs387906347
Biobank	rs387906347
1000 genomes	rs387906347
hgdp	rs387906347
ensembl	rs387906347
geneview	rs387906347
scholar	rs387906347
google	rs387906347
pharmgkb	rs387906347
gwascentral	rs387906347
openSNP	rs387906347
23andMe	rs387906347
SNPshot	rs387906347
SNPdbe	rs387906347
MSV3d	rs387906347
GWAS Ctlg	rs387906347

Max Magnitude

0

ClinVar
Risk	rs387906347(A;A)
Alt	rs387906347(A;A)
Reference	Rs387906347(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	GNE
CLNDBN	not specified not provided
Reversed	1
HGVS	NC_000009.11:g.36219853C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000349326.1, RCV000494055.1,