rs1057517961

Orientation

plus

Stabilized

plus

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

Make rs1057517961(G;G)

Make rs1057517961(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

66086758

Gene

ASL

is a	snp
is	mentioned by
dbSNP	rs1057517961
dbSNP (classic)	rs1057517961
ClinGen	rs1057517961
ebi	rs1057517961
HLI	rs1057517961
Exac	rs1057517961
Gnomad	rs1057517961
Varsome	rs1057517961
LitVar	rs1057517961
Map	rs1057517961
PheGenI	rs1057517961
Biobank	rs1057517961
1000 genomes	rs1057517961
hgdp	rs1057517961
ensembl	rs1057517961
geneview	rs1057517961
scholar	rs1057517961
google	rs1057517961
pharmgkb	rs1057517961
gwascentral	rs1057517961
openSNP	rs1057517961
23andMe	rs1057517961
SNPshot	rs1057517961
SNPdbe	rs1057517961
MSV3d	rs1057517961
GWAS Ctlg	rs1057517961

Max Magnitude

0

ClinVar
Risk	rs1057517961(G;G)
Alt	rs1057517961(G;G)
Reference	Rs1057517961(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ASL
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.65551745T>G
CLNSRC
CLNACC	RCV000414625.1,