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rs1064794459

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Chromosome5
Position93593738
GeneNR2F1
is asnp
is mentioned by
dbSNPrs1064794459
dbSNP (old)rs1064794459
ClinGenrs1064794459
ebirs1064794459
HLIrs1064794459
Exacrs1064794459
Gnomadrs1064794459
Varsomers1064794459
Maprs1064794459
PheGenIrs1064794459
Biobankrs1064794459
1000 genomesrs1064794459
hgdprs1064794459
ensemblrs1064794459
gopubmedrs1064794459
geneviewrs1064794459
scholarrs1064794459
googlers1064794459
pharmgkbrs1064794459
gwascentralrs1064794459
openSNPrs1064794459
23andMers1064794459
23andMe allrs1064794459
SNPshotrs1064794459
SNPdbers1064794459
MSV3drs1064794459
GWAS Ctlgrs1064794459
Max Magnitude0
ClinVar
Risk rs1064794459(-;-)
Alt rs1064794459(-;-)
Reference Rs1064794459(TCT;TCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NR2F1
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.92929444_92929446delTTC
CLNSRC
CLNACC RCV000478365.1,