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rs1064796097

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(ATTGA;ATTGA) 0 common in clinvar
Chromosome13
Position23334335
GeneSACS
is asnp
is mentioned by
dbSNPrs1064796097
dbSNP (old)rs1064796097
ClinGenrs1064796097
ebirs1064796097
HLIrs1064796097
Exacrs1064796097
Gnomadrs1064796097
Varsomers1064796097
Maprs1064796097
PheGenIrs1064796097
Biobankrs1064796097
1000 genomesrs1064796097
hgdprs1064796097
ensemblrs1064796097
gopubmedrs1064796097
geneviewrs1064796097
scholarrs1064796097
googlers1064796097
pharmgkbrs1064796097
gwascentralrs1064796097
openSNPrs1064796097
23andMers1064796097
23andMe allrs1064796097
SNPshotrs1064796097
SNPdbers1064796097
MSV3drs1064796097
GWAS Ctlgrs1064796097
Max Magnitude0
ClinVar
Risk rs1064796097(-;-)
Alt rs1064796097(-;-)
Reference Rs1064796097(ATTGA;ATTGA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SACS
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.23908474_23908478delTCAAT
CLNSRC
CLNACC RCV000479181.1,