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rs782349178

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs782349178(-;-)
Make rs782349178(-;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133352135
GeneSURF1
is asnp
is mentioned by
dbSNPrs782349178
dbSNP (classic)rs782349178
ClinGenrs782349178
ebirs782349178
HLIrs782349178
Exacrs782349178
Gnomadrs782349178
Varsomers782349178
LitVarrs782349178
Maprs782349178
PheGenIrs782349178
Biobankrs782349178
1000 genomesrs782349178
hgdprs782349178
ensemblrs782349178
geneviewrs782349178
scholarrs782349178
googlers782349178
pharmgkbrs782349178
gwascentralrs782349178
openSNPrs782349178
23andMers782349178
SNPshotrs782349178
SNPdbers782349178
MSV3drs782349178
GWAS Ctlgrs782349178
Max Magnitude0
ClinVar
Risk rs782349178(-;-)
Alt rs782349178(-;-)
Reference Rs782349178(TG;TG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136218990_136218991delTG
CLNSRC
CLNACC RCV000413343.1,