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rs1064793675

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome1
Position152311049
GeneFLG
is asnp
is mentioned by
dbSNPrs1064793675
dbSNP (classic)rs1064793675
ClinGenrs1064793675
ebirs1064793675
HLIrs1064793675
Exacrs1064793675
Gnomadrs1064793675
Varsomers1064793675
LitVarrs1064793675
Maprs1064793675
PheGenIrs1064793675
Biobankrs1064793675
1000 genomesrs1064793675
hgdprs1064793675
ensemblrs1064793675
geneviewrs1064793675
scholarrs1064793675
googlers1064793675
pharmgkbrs1064793675
gwascentralrs1064793675
openSNPrs1064793675
23andMers1064793675
23andMe allrs1064793675
SNPshotrs1064793675
SNPdbers1064793675
MSV3drs1064793675
GWAS Ctlgrs1064793675
Max Magnitude0
ClinVar
Risk rs1064793675(-;-)
Alt rs1064793675(-;-)
Reference Rs1064793675(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152283525delG
CLNSRC
CLNACC RCV000484364.1,