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rs1064795438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGATG;AGATG) 0 common in clinvar
Chromosome13
Position48342669
GeneRB1
is asnp
is mentioned by
dbSNPrs1064795438
dbSNP (classic)rs1064795438
ClinGenrs1064795438
ebirs1064795438
HLIrs1064795438
Exacrs1064795438
Gnomadrs1064795438
Varsomers1064795438
LitVarrs1064795438
Maprs1064795438
PheGenIrs1064795438
Biobankrs1064795438
1000 genomesrs1064795438
hgdprs1064795438
ensemblrs1064795438
geneviewrs1064795438
scholarrs1064795438
googlers1064795438
pharmgkbrs1064795438
gwascentralrs1064795438
openSNPrs1064795438
23andMers1064795438
SNPshotrs1064795438
SNPdbers1064795438
MSV3drs1064795438
GWAS Ctlgrs1064795438
Max Magnitude0
ClinVar
Risk rs1064795438(-;-)
Alt rs1064795438(-;-)
Reference Rs1064795438(AGATG;AGATG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RB1
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.48916805_48916809delAGATG
CLNSRC
CLNACC RCV000480648.1,