rs1064795636

Orientation

minus

Stabilized

minus

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

Chromosome

9

Position

127824896

Gene	ENG, LOC105379841

is a	snp
is	mentioned by
dbSNP	rs1064795636
dbSNP (classic)	rs1064795636
ClinGen	rs1064795636
ebi	rs1064795636
HLI	rs1064795636
Exac	rs1064795636
Gnomad	rs1064795636
Varsome	rs1064795636
LitVar	rs1064795636
Map	rs1064795636
PheGenI	rs1064795636
Biobank	rs1064795636
1000 genomes	rs1064795636
hgdp	rs1064795636
ensembl	rs1064795636
geneview	rs1064795636
scholar	rs1064795636
google	rs1064795636
pharmgkb	rs1064795636
gwascentral	rs1064795636
openSNP	rs1064795636
23andMe	rs1064795636
SNPshot	rs1064795636
SNPdbe	rs1064795636
MSV3d	rs1064795636
GWAS Ctlg	rs1064795636

Max Magnitude

0

ClinVar
Risk	rs1064795636(-;-)
Alt	rs1064795636(-;-)
Reference	Rs1064795636(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ENG
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130587175delG
CLNSRC
CLNACC	RCV000481830.1,