Have questions? Visit https://www.reddit.com/r/SNPedia

rs1064793863

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome2
Position47414282
GeneMSH2
is asnp
is mentioned by
dbSNPrs1064793863
dbSNP (old)rs1064793863
ClinGenrs1064793863
ebirs1064793863
HLIrs1064793863
Exacrs1064793863
Gnomadrs1064793863
Varsomers1064793863
Maprs1064793863
PheGenIrs1064793863
Biobankrs1064793863
1000 genomesrs1064793863
hgdprs1064793863
ensemblrs1064793863
gopubmedrs1064793863
geneviewrs1064793863
scholarrs1064793863
googlers1064793863
pharmgkbrs1064793863
gwascentralrs1064793863
openSNPrs1064793863
23andMers1064793863
23andMe allrs1064793863
SNPshotrs1064793863
SNPdbers1064793863
MSV3drs1064793863
GWAS Ctlgrs1064793863
Max Magnitude0
ClinVar
Risk rs1064793863(TGTACCGCAGATT;TGTACCGCAGATT)
Alt rs1064793863(TGTACCGCAGATT;TGTACCGCAGATT)
Reference Rs1064793863(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47641421_47641422insTGTACCGCAGATT
CLNSRC
CLNACC RCV000485656.1,