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rs1064795660

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GT;GT) 0 common in clinvar
Chromosome17
Position28534539
GeneFOXN1
is asnp
is mentioned by
dbSNPrs1064795660
dbSNP (old)rs1064795660
ClinGenrs1064795660
ebirs1064795660
HLIrs1064795660
Exacrs1064795660
Gnomadrs1064795660
Varsomers1064795660
Maprs1064795660
PheGenIrs1064795660
Biobankrs1064795660
1000 genomesrs1064795660
hgdprs1064795660
ensemblrs1064795660
gopubmedrs1064795660
geneviewrs1064795660
scholarrs1064795660
googlers1064795660
pharmgkbrs1064795660
gwascentralrs1064795660
openSNPrs1064795660
23andMers1064795660
23andMe allrs1064795660
SNPshotrs1064795660
SNPdbers1064795660
MSV3drs1064795660
GWAS Ctlgrs1064795660
Max Magnitude0
ClinVar
Risk rs1064795660(AG;AG)
Alt rs1064795660(AG;AG)
Reference Rs1064795660(GT;GT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXN1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.26861557_26861558delGTinsAG
CLNSRC
CLNACC RCV000480185.1,