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rs1085307956

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome7
Position97853112
GeneASNS
is asnp
is mentioned by
dbSNPrs1085307956
dbSNP (old)rs1085307956
ClinGenrs1085307956
ebirs1085307956
HLIrs1085307956
Exacrs1085307956
Gnomadrs1085307956
Varsomers1085307956
Maprs1085307956
PheGenIrs1085307956
Biobankrs1085307956
1000 genomesrs1085307956
hgdprs1085307956
ensemblrs1085307956
gopubmedrs1085307956
geneviewrs1085307956
scholarrs1085307956
googlers1085307956
pharmgkbrs1085307956
gwascentralrs1085307956
openSNPrs1085307956
23andMers1085307956
23andMe allrs1085307956
SNPshotrs1085307956
SNPdbers1085307956
MSV3drs1085307956
GWAS Ctlgrs1085307956
Max Magnitude0
ClinVar
Risk rs1085307956(A;A)
Alt rs1085307956(A;A)
Reference Rs1085307956(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ASNS
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.97482424G>T
CLNSRC
CLNACC RCV000489606.1,