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rs782488388

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs782488388(-;-)
Make rs782488388(-;AGACGT)
Make rs782488388(AGACGT;AGACGT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133352075
GeneSURF1
is asnp
is mentioned by
dbSNPrs782488388
ebirs782488388
HLIrs782488388
Exacrs782488388
Varsomers782488388
Maprs782488388
PheGenIrs782488388
hapmaprs782488388
1000 genomesrs782488388
hgdprs782488388
ensemblrs782488388
gopubmedrs782488388
geneviewrs782488388
scholarrs782488388
googlers782488388
pharmgkbrs782488388
gwascentralrs782488388
openSNPrs782488388
23andMers782488388
23andMe allrs782488388
SNP Nexus

SNPshotrs782488388
SNPdbers782488388
MSV3drs782488388
GWAS Ctlgrs782488388
Max Magnitude0
ClinVar
Risk rs782488388(CT,CTGCAGA;CT,CTGCAGA)
Alt rs782488388(CT,CTGCAGA;CT,CTGCAGA)
Reference rs782488388(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136218931_136218936dupTGCAGA
CLNSRC
CLNACC RCV000196024.1,