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rs764356037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764356037(C;C)
Make rs764356037(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position66089335
GeneASL
is asnp
is mentioned by
dbSNPrs764356037
dbSNP (classic)rs764356037
ClinGenrs764356037
ebirs764356037
HLIrs764356037
Exacrs764356037
Gnomadrs764356037
Varsomers764356037
LitVarrs764356037
Maprs764356037
PheGenIrs764356037
Biobankrs764356037
1000 genomesrs764356037
hgdprs764356037
ensemblrs764356037
geneviewrs764356037
scholarrs764356037
googlers764356037
pharmgkbrs764356037
gwascentralrs764356037
openSNPrs764356037
23andMers764356037
23andMe allrs764356037
SNPshotrs764356037
SNPdbers764356037
MSV3drs764356037
GWAS Ctlgrs764356037
Max Magnitude0
ClinVar
Risk rs764356037(C;C)
Alt rs764356037(C;C)
Reference Rs764356037(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASL
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.65554322G>C
CLNSRC
CLNACC RCV000489610.1,