rs773073663

Orientation

plus

Stabilized

plus

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

Make rs773073663(C;T)

Make rs773073663(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127819899

Gene	ENG, LOC102723566

is a	snp
is	mentioned by
dbSNP	rs773073663
dbSNP (classic)	rs773073663
ClinGen	rs773073663
ebi	rs773073663
HLI	rs773073663
Exac	rs773073663
Gnomad	rs773073663
Varsome	rs773073663
LitVar	rs773073663
Map	rs773073663
PheGenI	rs773073663
Biobank	rs773073663
1000 genomes	rs773073663
hgdp	rs773073663
ensembl	rs773073663
geneview	rs773073663
scholar	rs773073663
google	rs773073663
pharmgkb	rs773073663
gwascentral	rs773073663
openSNP	rs773073663
23andMe	rs773073663
SNPshot	rs773073663
SNPdbe	rs773073663
MSV3d	rs773073663
GWAS Ctlg	rs773073663

Max Magnitude

0

ClinVar
Risk	rs773073663(A;A) rs773073663(T;T)
Alt	rs773073663(A;A) rs773073663(T;T)
Reference	Rs773073663(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG LOC102723566
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.130582178C>T
CLNSRC
CLNACC	RCV000196088.1,