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rs138726443

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs138726443(A;A)
Make rs138726443(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152307547
GeneFLG
is asnp
is mentioned by
dbSNPrs138726443
dbSNP (old)rs138726443
ClinGenrs138726443
ebirs138726443
HLIrs138726443
Exacrs138726443
Gnomadrs138726443
Varsomers138726443
LitVarrs138726443
Maprs138726443
PheGenIrs138726443
Biobankrs138726443
1000 genomesrs138726443
hgdprs138726443
ensemblrs138726443
gopubmedrs138726443
geneviewrs138726443
scholarrs138726443
googlers138726443
pharmgkbrs138726443
gwascentralrs138726443
openSNPrs138726443
23andMers138726443
23andMe allrs138726443
SNPshotrs138726443
SNPdbers138726443
MSV3drs138726443
GWAS Ctlgrs138726443
Max Magnitude0
ClinVar
Risk rs138726443(A;A) rs138726443(C;C) rs138726443(T;T)
Alt rs138726443(A;A) rs138726443(C;C) rs138726443(T;T)
Reference Rs138726443(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152280023G>A
CLNSRC
CLNACC RCV000255655.2,