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rs1064793391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome3
Position4417183
GeneSUMF1
is asnp
is mentioned by
dbSNPrs1064793391
dbSNP (classic)rs1064793391
ClinGenrs1064793391
ebirs1064793391
HLIrs1064793391
Exacrs1064793391
Gnomadrs1064793391
Varsomers1064793391
LitVarrs1064793391
Maprs1064793391
PheGenIrs1064793391
Biobankrs1064793391
1000 genomesrs1064793391
hgdprs1064793391
ensemblrs1064793391
geneviewrs1064793391
scholarrs1064793391
googlers1064793391
pharmgkbrs1064793391
gwascentralrs1064793391
openSNPrs1064793391
23andMers1064793391
23andMe allrs1064793391
SNPshotrs1064793391
SNPdbers1064793391
MSV3drs1064793391
GWAS Ctlgrs1064793391
Max Magnitude0
ClinVar
Risk rs1064793391(G;G)
Alt rs1064793391(G;G)
Reference Rs1064793391(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SUMF1
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.4458867T>C
CLNSRC
CLNACC RCV000481019.1,