rs863223536

Orientation

minus

Stabilized

minus

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

Make rs863223536(A;T)

Make rs863223536(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127818832

Gene	ENG, LOC102723566

is a	snp
is	mentioned by
dbSNP	rs863223536
dbSNP (classic)	rs863223536
ClinGen	rs863223536
ebi	rs863223536
HLI	rs863223536
Exac	rs863223536
Gnomad	rs863223536
Varsome	rs863223536
LitVar	rs863223536
Map	rs863223536
PheGenI	rs863223536
Biobank	rs863223536
1000 genomes	rs863223536
hgdp	rs863223536
ensembl	rs863223536
geneview	rs863223536
scholar	rs863223536
google	rs863223536
pharmgkb	rs863223536
gwascentral	rs863223536
openSNP	rs863223536
23andMe	rs863223536
SNPshot	rs863223536
SNPdbe	rs863223536
MSV3d	rs863223536
GWAS Ctlg	rs863223536

Max Magnitude

0

ClinVar
Risk	rs863223536(T;T)
Alt	rs863223536(T;T)
Reference	Rs863223536(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG LOC102723566
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130581111T>A
CLNSRC
CLNACC	RCV000198335.1,