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rs199885226

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs199885226(G;T)
Make rs199885226(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152314107
GeneFLG, FLG-AS1
is asnp
is mentioned by
dbSNPrs199885226
dbSNP (old)rs199885226
ClinGenrs199885226
ebirs199885226
HLIrs199885226
Exacrs199885226
Gnomadrs199885226
Varsomers199885226
Maprs199885226
PheGenIrs199885226
Biobankrs199885226
1000 genomesrs199885226
hgdprs199885226
ensemblrs199885226
gopubmedrs199885226
geneviewrs199885226
scholarrs199885226
googlers199885226
pharmgkbrs199885226
gwascentralrs199885226
openSNPrs199885226
23andMers199885226
23andMe allrs199885226
SNPshotrs199885226
SNPdbers199885226
MSV3drs199885226
GWAS Ctlgrs199885226
Max Magnitude0
ClinVar
Risk rs199885226(C;C) rs199885226(T;T)
Alt rs199885226(C;C) rs199885226(T;T)
Reference Rs199885226(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG FLG-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152286583G>T
CLNSRC
CLNACC RCV000358958.1,