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rs782490558

From SNPedia

Orientationplus
Make rs782490558(-;-)
Make rs782490558(-;CT)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position133352101
GeneSURF1
is asnp
is mentioned by
dbSNPrs782490558
ebirs782490558
HLIrs782490558
Exacrs782490558
Varsomers782490558
Maprs782490558
PheGenIrs782490558
hapmaprs782490558
1000 genomesrs782490558
hgdprs782490558
ensemblrs782490558
gopubmedrs782490558
geneviewrs782490558
scholarrs782490558
googlers782490558
pharmgkbrs782490558
gwascentralrs782490558
openSNPrs782490558
23andMers782490558
23andMe allrs782490558
SNP Nexus

SNPshotrs782490558
SNPdbers782490558
MSV3drs782490558
GWAS Ctlgrs782490558
Max Magnitude
ClinVar
Risk rs782490558(;)
Alt rs782490558(;)
Reference rs782490558(CT;CT)
Significance Pathogenic
Disease not provided
Variation info
Gene SURF1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.136218956_136218957delCT
CLNSRC
CLNACC RCV000198901.1,