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rs761877421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs761877421(-;-)
Make rs761877421(-;TC)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152313588
GeneFLG, FLG-AS1
is asnp
is mentioned by
dbSNPrs761877421
dbSNP (classic)rs761877421
ClinGenrs761877421
ebirs761877421
HLIrs761877421
Exacrs761877421
Gnomadrs761877421
Varsomers761877421
LitVarrs761877421
Maprs761877421
PheGenIrs761877421
Biobankrs761877421
1000 genomesrs761877421
hgdprs761877421
ensemblrs761877421
geneviewrs761877421
scholarrs761877421
googlers761877421
pharmgkbrs761877421
gwascentralrs761877421
openSNPrs761877421
23andMers761877421
SNPshotrs761877421
SNPdbers761877421
MSV3drs761877421
GWAS Ctlgrs761877421
Max Magnitude0
ClinVar
Risk rs761877421(-;-)
Alt rs761877421(-;-)
Reference Rs761877421(TC;TC)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG FLG-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152286064_152286065delTC
CLNSRC
CLNACC RCV000490026.1,