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rs74129447

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs74129447(C;T)
Make rs74129447(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position152303313
GeneFLG
is asnp
is mentioned by
dbSNPrs74129447
ebirs74129447
HLIrs74129447
Exacrs74129447
Varsomers74129447
Maprs74129447
PheGenIrs74129447
hapmaprs74129447
1000 genomesrs74129447
hgdprs74129447
ensemblrs74129447
gopubmedrs74129447
geneviewrs74129447
scholarrs74129447
googlers74129447
pharmgkbrs74129447
gwascentralrs74129447
openSNPrs74129447
23andMers74129447
23andMe allrs74129447
SNP Nexus

SNPshotrs74129447
SNPdbers74129447
MSV3drs74129447
GWAS Ctlgrs74129447
Max Magnitude0
ClinVar
Risk rs74129447(A,T;A,T)
Alt rs74129447(A,T;A,T)
Reference rs74129447(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152275789C>T
CLNSRC
CLNACC RCV000171158.1,