rs776384541

Orientation

plus

Stabilized

plus

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

Make rs776384541(C;T)

Make rs776384541(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

36217529

Gene

GNE

is a	snp
is	mentioned by
dbSNP	rs776384541
dbSNP (classic)	rs776384541
ClinGen	rs776384541
ebi	rs776384541
HLI	rs776384541
Exac	rs776384541
Gnomad	rs776384541
Varsome	rs776384541
LitVar	rs776384541
Map	rs776384541
PheGenI	rs776384541
Biobank	rs776384541
1000 genomes	rs776384541
hgdp	rs776384541
ensembl	rs776384541
geneview	rs776384541
scholar	rs776384541
google	rs776384541
pharmgkb	rs776384541
gwascentral	rs776384541
openSNP	rs776384541
23andMe	rs776384541
SNPshot	rs776384541
SNPdbe	rs776384541
MSV3d	rs776384541
GWAS Ctlg	rs776384541

Max Magnitude

0

ClinVar
Risk	rs776384541(T;T)
Alt	rs776384541(T;T)
Reference	Rs776384541(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GNE
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.36217526C>T
CLNSRC
CLNACC	RCV000322771.1,