rs764356037

Orientation

plus

Stabilized

plus

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

Make rs764356037(C;C)

Make rs764356037(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

66089335

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs764356037
dbSNP (classic)	rs764356037
ClinGen	rs764356037
ebi	rs764356037
HLI	rs764356037
Exac	rs764356037
Gnomad	rs764356037
Varsome	rs764356037
LitVar	rs764356037
Map	rs764356037
PheGenI	rs764356037
Biobank	rs764356037
1000 genomes	rs764356037
hgdp	rs764356037
ensembl	rs764356037
geneview	rs764356037
scholar	rs764356037
google	rs764356037
pharmgkb	rs764356037
gwascentral	rs764356037
openSNP	rs764356037
23andMe	rs764356037
SNPshot	rs764356037
SNPdbe	rs764356037
MSV3d	rs764356037
GWAS Ctlg	rs764356037

Max Magnitude

0

ClinVar
Risk	rs764356037(C;C)
Alt	rs764356037(C;C)
Reference	Rs764356037(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ASL
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.65554322G>C
CLNSRC
CLNACC	RCV000489610.1,