rs561367199

Orientation

plus

Stabilized

plus

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

Make rs561367199(A;A)

Make rs561367199(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

66082920

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs561367199
dbSNP (classic)	rs561367199
ClinGen	rs561367199
ebi	rs561367199
HLI	rs561367199
Exac	rs561367199
Gnomad	rs561367199
Varsome	rs561367199
LitVar	rs561367199
Map	rs561367199
PheGenI	rs561367199
Biobank	rs561367199
1000 genomes	rs561367199
hgdp	rs561367199
ensembl	rs561367199
geneview	rs561367199
scholar	rs561367199
google	rs561367199
pharmgkb	rs561367199
gwascentral	rs561367199
openSNP	rs561367199
23andMe	rs561367199
SNPshot	rs561367199
SNPdbe	rs561367199
MSV3d	rs561367199
GWAS Ctlg	rs561367199

Max Magnitude

0

ClinVar
Risk	rs561367199(A;A)
Alt	rs561367199(A;A)
Reference	Rs561367199(G;G)
Significance	Probable-Pathogenic
Disease	not specified not provided
Variation	info
Gene	ASL
CLNDBN	not specified not provided
Reversed	0
HGVS	NC_000007.13:g.65547907G>A
CLNSRC
CLNACC	RCV000272723.1, RCV000493464.1,