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rs782024654

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs782024654(A;G)
Make rs782024654(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position133354713
GeneSURF1, SURF2
is asnp
is mentioned by
dbSNPrs782024654
dbSNP (classic)rs782024654
ClinGenrs782024654
ebirs782024654
HLIrs782024654
Exacrs782024654
Gnomadrs782024654
Varsomers782024654
LitVarrs782024654
Maprs782024654
PheGenIrs782024654
Biobankrs782024654
1000 genomesrs782024654
hgdprs782024654
ensemblrs782024654
geneviewrs782024654
scholarrs782024654
googlers782024654
pharmgkbrs782024654
gwascentralrs782024654
openSNPrs782024654
23andMers782024654
SNPshotrs782024654
SNPdbers782024654
MSV3drs782024654
GWAS Ctlgrs782024654
Max Magnitude0
ClinVar
Risk rs782024654(G;G)
Alt rs782024654(G;G)
Reference Rs782024654(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SURF2 SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136221568A>G
CLNSRC
CLNACC RCV000437222.1,