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rs397507563

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397507563(-;-)
Make rs397507563(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152311184
GeneFLG
is asnp
is mentioned by
dbSNPrs397507563
dbSNP (classic)rs397507563
ClinGenrs397507563
ebirs397507563
HLIrs397507563
Exacrs397507563
Gnomadrs397507563
Varsomers397507563
LitVarrs397507563
Maprs397507563
PheGenIrs397507563
Biobankrs397507563
1000 genomesrs397507563
hgdprs397507563
ensemblrs397507563
geneviewrs397507563
scholarrs397507563
googlers397507563
pharmgkbrs397507563
gwascentralrs397507563
openSNPrs397507563
23andMers397507563
23andMe allrs397507563
SNPshotrs397507563
SNPdbers397507563
MSV3drs397507563
GWAS Ctlgrs397507563
Max Magnitude0
ClinVar
Risk rs397507563(-;-)
Alt rs397507563(-;-)
Reference Rs397507563(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152283660delC
CLNSRC
CLNACC RCV000479326.1,