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rs374588791

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs374588791(C;T)
Make rs374588791(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152307622
GeneFLG
is asnp
is mentioned by
dbSNPrs374588791
dbSNP (old)rs374588791
ClinGenrs374588791
ebirs374588791
HLIrs374588791
Exacrs374588791
Varsomers374588791
Maprs374588791
PheGenIrs374588791
Biobankrs374588791
1000 genomesrs374588791
hgdprs374588791
ensemblrs374588791
gopubmedrs374588791
geneviewrs374588791
scholarrs374588791
googlers374588791
pharmgkbrs374588791
gwascentralrs374588791
openSNPrs374588791
23andMers374588791
23andMe allrs374588791
SNP Nexus

SNPshotrs374588791
SNPdbers374588791
MSV3drs374588791
GWAS Ctlgrs374588791
Max Magnitude0
ClinVar
Risk rs374588791(A;A) rs374588791(T;T)
Alt rs374588791(A;A) rs374588791(T;T)
Reference Rs374588791(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152280098C>A
CLNSRC
CLNACC RCV000255031.1,