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rs1085307952

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome7
Position66089096
GeneASL
is asnp
is mentioned by
dbSNPrs1085307952
dbSNP (old)rs1085307952
ClinGenrs1085307952
ebirs1085307952
HLIrs1085307952
Exacrs1085307952
Gnomadrs1085307952
Varsomers1085307952
Maprs1085307952
PheGenIrs1085307952
Biobankrs1085307952
1000 genomesrs1085307952
hgdprs1085307952
ensemblrs1085307952
gopubmedrs1085307952
geneviewrs1085307952
scholarrs1085307952
googlers1085307952
pharmgkbrs1085307952
gwascentralrs1085307952
openSNPrs1085307952
23andMers1085307952
23andMe allrs1085307952
SNPshotrs1085307952
SNPdbers1085307952
MSV3drs1085307952
GWAS Ctlgrs1085307952
Max Magnitude0
ClinVar
Risk rs1085307952(A;A)
Alt rs1085307952(A;A)
Reference Rs1085307952(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASL
CLNDBN not provided
Reversed 0
HGVS NC_000007.13:g.65554083G>A
CLNSRC
CLNACC RCV000489046.1,