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rs782289759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs782289759(-;GCAG)
Make rs782289759(GCAG;GCAG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133352707
GeneSURF1
is asnp
is mentioned by
dbSNPrs782289759
dbSNP (classic)rs782289759
ClinGenrs782289759
ebirs782289759
HLIrs782289759
Exacrs782289759
Gnomadrs782289759
Varsomers782289759
LitVarrs782289759
Maprs782289759
PheGenIrs782289759
Biobankrs782289759
1000 genomesrs782289759
hgdprs782289759
ensemblrs782289759
geneviewrs782289759
scholarrs782289759
googlers782289759
pharmgkbrs782289759
gwascentralrs782289759
openSNPrs782289759
23andMers782289759
SNPshotrs782289759
SNPdbers782289759
MSV3drs782289759
GWAS Ctlgrs782289759
Max Magnitude0
ClinVar
Risk rs782289759(GCAG;GCAG)
Alt rs782289759(GCAG;GCAG)
Reference Rs782289759(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136219562_136219563insGCAG
CLNSRC
CLNACC RCV000478177.1,