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rs1064795469

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome13
Position32337560
is asnp
is mentioned by
dbSNPrs1064795469
dbSNP (old)rs1064795469
ClinGenrs1064795469
ebirs1064795469
HLIrs1064795469
Exacrs1064795469
Gnomadrs1064795469
Varsomers1064795469
Maprs1064795469
PheGenIrs1064795469
Biobankrs1064795469
1000 genomesrs1064795469
hgdprs1064795469
ensemblrs1064795469
gopubmedrs1064795469
geneviewrs1064795469
scholarrs1064795469
googlers1064795469
pharmgkbrs1064795469
gwascentralrs1064795469
openSNPrs1064795469
23andMers1064795469
23andMe allrs1064795469
SNPshotrs1064795469
SNPdbers1064795469
MSV3drs1064795469
GWAS Ctlgrs1064795469
Max Magnitude0
ClinVar
Risk rs1064795469(TAATTGCAGTCAATTAATA;TAATTGCAGTCAATTAATA)
Alt rs1064795469(TAATTGCAGTCAATTAATA;TAATTGCAGTCAATTAATA)
Reference Rs1064795469(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.32911697_32911698insTAATTGCAGTCAATTAATA
CLNSRC
CLNACC RCV000481346.1,