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rs1057517961

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057517961(G;G)
Make rs1057517961(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66086758
GeneASL
is asnp
is mentioned by
dbSNPrs1057517961
dbSNP (old)rs1057517961
ClinGenrs1057517961
ebirs1057517961
HLIrs1057517961
Exacrs1057517961
Gnomadrs1057517961
Varsomers1057517961
Maprs1057517961
PheGenIrs1057517961
Biobankrs1057517961
1000 genomesrs1057517961
hgdprs1057517961
ensemblrs1057517961
gopubmedrs1057517961
geneviewrs1057517961
scholarrs1057517961
googlers1057517961
pharmgkbrs1057517961
gwascentralrs1057517961
openSNPrs1057517961
23andMers1057517961
23andMe allrs1057517961
SNPshotrs1057517961
SNPdbers1057517961
MSV3drs1057517961
GWAS Ctlgrs1057517961
Max Magnitude0
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,