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rs1064794299

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Chromosome1
Position183567223
GeneNCF2
is asnp
is mentioned by
dbSNPrs1064794299
dbSNP (old)rs1064794299
ClinGenrs1064794299
ebirs1064794299
HLIrs1064794299
Exacrs1064794299
Gnomadrs1064794299
Varsomers1064794299
Maprs1064794299
PheGenIrs1064794299
Biobankrs1064794299
1000 genomesrs1064794299
hgdprs1064794299
ensemblrs1064794299
gopubmedrs1064794299
geneviewrs1064794299
scholarrs1064794299
googlers1064794299
pharmgkbrs1064794299
gwascentralrs1064794299
openSNPrs1064794299
23andMers1064794299
23andMe allrs1064794299
SNPshotrs1064794299
SNPdbers1064794299
MSV3drs1064794299
GWAS Ctlgrs1064794299
Max Magnitude0
ClinVar
Risk rs1064794299(-;-)
Alt rs1064794299(-;-)
Reference Rs1064794299(AC;AC)
Significance Pathogenic
Disease not provided
Variation info
Gene NCF2
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.183536358_183536359delGT
CLNSRC
CLNACC RCV000482820.1,