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rs749083759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs749083759(A;A)
Make rs749083759(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152303917
GeneFLG
is asnp
is mentioned by
dbSNPrs749083759
dbSNP (classic)rs749083759
ClinGenrs749083759
ebirs749083759
HLIrs749083759
Exacrs749083759
Gnomadrs749083759
Varsomers749083759
LitVarrs749083759
Maprs749083759
PheGenIrs749083759
Biobankrs749083759
1000 genomesrs749083759
hgdprs749083759
ensemblrs749083759
geneviewrs749083759
scholarrs749083759
googlers749083759
pharmgkbrs749083759
gwascentralrs749083759
openSNPrs749083759
23andMers749083759
SNPshotrs749083759
SNPdbers749083759
MSV3drs749083759
GWAS Ctlgrs749083759
Max Magnitude0
ClinVar
Risk rs749083759(A;A) rs749083759(C;C)
Alt rs749083759(A;A) rs749083759(C;C)
Reference Rs749083759(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152276393G>A
CLNSRC
CLNACC RCV000493067.1,