rs761651320

Orientation

plus

Stabilized

plus

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

Make rs761651320(C;T)

Make rs761651320(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

66087368

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs761651320
dbSNP (classic)	rs761651320
ClinGen	rs761651320
ebi	rs761651320
HLI	rs761651320
Exac	rs761651320
Gnomad	rs761651320
Varsome	rs761651320
LitVar	rs761651320
Map	rs761651320
PheGenI	rs761651320
Biobank	rs761651320
1000 genomes	rs761651320
hgdp	rs761651320
ensembl	rs761651320
geneview	rs761651320
scholar	rs761651320
google	rs761651320
pharmgkb	rs761651320
gwascentral	rs761651320
openSNP	rs761651320
23andMe	rs761651320
SNPshot	rs761651320
SNPdbe	rs761651320
MSV3d	rs761651320
GWAS Ctlg	rs761651320

Max Magnitude

0

ClinVar
Risk	rs761651320(T;T)
Alt	rs761651320(T;T)
Reference	Rs761651320(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ASL
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.65552355C>T
CLNSRC
CLNACC	RCV000489563.1,