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rs546871592

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs546871592(A;A)
Make rs546871592(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152303251
GeneFLG
is asnp
is mentioned by
dbSNPrs546871592
dbSNP (old)rs546871592
ClinGenrs546871592
ebirs546871592
HLIrs546871592
Exacrs546871592
Gnomadrs546871592
Varsomers546871592
Maprs546871592
PheGenIrs546871592
Biobankrs546871592
1000 genomesrs546871592
hgdprs546871592
ensemblrs546871592
gopubmedrs546871592
geneviewrs546871592
scholarrs546871592
googlers546871592
pharmgkbrs546871592
gwascentralrs546871592
openSNPrs546871592
23andMers546871592
23andMe allrs546871592
SNP Nexus

SNPshotrs546871592
SNPdbers546871592
MSV3drs546871592
GWAS Ctlgrs546871592
Max Magnitude0
ClinVar
Risk rs546871592(A;A)
Alt rs546871592(A;A)
Reference Rs546871592(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152275727G>A
CLNSRC
CLNACC RCV000493665.1,