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rs777181377

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs777181377(A;A)
Make rs777181377(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152312668
GeneFLG, FLG-AS1
is asnp
is mentioned by
dbSNPrs777181377
dbSNP (classic)rs777181377
ClinGenrs777181377
ebirs777181377
HLIrs777181377
Exacrs777181377
Gnomadrs777181377
Varsomers777181377
LitVarrs777181377
Maprs777181377
PheGenIrs777181377
Biobankrs777181377
1000 genomesrs777181377
hgdprs777181377
ensemblrs777181377
geneviewrs777181377
scholarrs777181377
googlers777181377
pharmgkbrs777181377
gwascentralrs777181377
openSNPrs777181377
23andMers777181377
SNPshotrs777181377
SNPdbers777181377
MSV3drs777181377
GWAS Ctlgrs777181377
Max Magnitude0
ClinVar
Risk rs777181377(A;A)
Alt rs777181377(A;A)
Reference Rs777181377(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG FLG-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152285144G>A
CLNSRC
CLNACC RCV000293346.1,