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rs782623477

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs782623477(A;A)
Make rs782623477(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position133352509
GeneSURF1
is asnp
is mentioned by
dbSNPrs782623477
dbSNP (classic)rs782623477
ClinGenrs782623477
ebirs782623477
HLIrs782623477
Exacrs782623477
Gnomadrs782623477
Varsomers782623477
LitVarrs782623477
Maprs782623477
PheGenIrs782623477
Biobankrs782623477
1000 genomesrs782623477
hgdprs782623477
ensemblrs782623477
geneviewrs782623477
scholarrs782623477
googlers782623477
pharmgkbrs782623477
gwascentralrs782623477
openSNPrs782623477
23andMers782623477
SNPshotrs782623477
SNPdbers782623477
MSV3drs782623477
GWAS Ctlgrs782623477
Max Magnitude0
ClinVar
Risk rs782623477(A;A)
Alt rs782623477(A;A)
Reference Rs782623477(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136219364G>A
CLNSRC
CLNACC RCV000321649.1,