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rs1064795702

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
ChromosomeX
Position136207937
GeneFHL1
is asnp
is mentioned by
dbSNPrs1064795702
dbSNP (old)rs1064795702
ClinGenrs1064795702
ebirs1064795702
HLIrs1064795702
Exacrs1064795702
Gnomadrs1064795702
Varsomers1064795702
Maprs1064795702
PheGenIrs1064795702
Biobankrs1064795702
1000 genomesrs1064795702
hgdprs1064795702
ensemblrs1064795702
gopubmedrs1064795702
geneviewrs1064795702
scholarrs1064795702
googlers1064795702
pharmgkbrs1064795702
gwascentralrs1064795702
openSNPrs1064795702
23andMers1064795702
23andMe allrs1064795702
SNPshotrs1064795702
SNPdbers1064795702
MSV3drs1064795702
GWAS Ctlgrs1064795702
Max Magnitude0
ClinVar
Risk rs1064795702(-;-)
Alt rs1064795702(-;-)
Reference Rs1064795702(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FHL1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.135290096delC
CLNSRC
CLNACC RCV000479357.1,