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rs1057141162

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66086758
GeneASL
is asnp
is mentioned by
dbSNPrs1057141162
dbSNP (old)rs1057141162
ClinGenrs1057141162
ebirs1057141162
HLIrs1057141162
Exacrs1057141162
Gnomadrs1057141162
Varsomers1057141162
LitVarrs1057141162
Maprs1057141162
PheGenIrs1057141162
Biobankrs1057141162
1000 genomesrs1057141162
hgdprs1057141162
ensemblrs1057141162
gopubmedrs1057141162
geneviewrs1057141162
scholarrs1057141162
googlers1057141162
pharmgkbrs1057141162
gwascentralrs1057141162
openSNPrs1057141162
23andMers1057141162
23andMe allrs1057141162
SNPshotrs1057141162
SNPdbers1057141162
MSV3drs1057141162
GWAS Ctlgrs1057141162
Max Magnitude0
ClinVar
Risk rs1057141162(G;G)
Alt rs1057141162(G;G)
Reference Rs1057141162(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.65551745T>G
CLNSRC
CLNACC RCV000414625.1,