Have questions? Visit https://www.reddit.com/r/SNPedia

rs760831749

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0 common genotype
(TG;TG) 0 common in clinvar
Make rs760831749(-;-)
Make rs760831749(-;TG)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152307618
GeneFLG
is asnp
is mentioned by
dbSNPrs760831749
dbSNP (classic)rs760831749
ClinGenrs760831749
ebirs760831749
HLIrs760831749
Exacrs760831749
Gnomadrs760831749
Varsomers760831749
LitVarrs760831749
Maprs760831749
PheGenIrs760831749
Biobankrs760831749
1000 genomesrs760831749
hgdprs760831749
ensemblrs760831749
geneviewrs760831749
scholarrs760831749
googlers760831749
pharmgkbrs760831749
gwascentralrs760831749
openSNPrs760831749
23andMers760831749
SNPshotrs760831749
SNPdbers760831749
MSV3drs760831749
GWAS Ctlgrs760831749
Max Magnitude0
ClinVar
Risk rs760831749(-;-)
Alt rs760831749(-;-)
Reference Rs760831749(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152280094_152280095delTG
CLNSRC
CLNACC RCV000256154.1,