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rs1085307810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CAGA;CAGA) 0 common in clinvar
Chromosome2
Position27232196
GeneCAD
is asnp
is mentioned by
dbSNPrs1085307810
dbSNP (classic)rs1085307810
ClinGenrs1085307810
ebirs1085307810
HLIrs1085307810
Exacrs1085307810
Gnomadrs1085307810
Varsomers1085307810
LitVarrs1085307810
Maprs1085307810
PheGenIrs1085307810
Biobankrs1085307810
1000 genomesrs1085307810
hgdprs1085307810
ensemblrs1085307810
geneviewrs1085307810
scholarrs1085307810
googlers1085307810
pharmgkbrs1085307810
gwascentralrs1085307810
openSNPrs1085307810
23andMers1085307810
23andMe allrs1085307810
SNPshotrs1085307810
SNPdbers1085307810
MSV3drs1085307810
GWAS Ctlgrs1085307810
Max Magnitude0
ClinVar
Risk rs1085307810(-;-)
Alt rs1085307810(-;-)
Reference Rs1085307810(CAGA;CAGA)
Significance Pathogenic
Disease not provided
Variation info
Gene CAD
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.27455064_27455067delGACA
CLNSRC
CLNACC RCV000490138.1,