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rs1057518212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518212(C;G)
Make rs1057518212(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152303358
GeneFLG
is asnp
is mentioned by
dbSNPrs1057518212
dbSNP (classic)rs1057518212
ClinGenrs1057518212
ebirs1057518212
HLIrs1057518212
Exacrs1057518212
Gnomadrs1057518212
Varsomers1057518212
LitVarrs1057518212
Maprs1057518212
PheGenIrs1057518212
Biobankrs1057518212
1000 genomesrs1057518212
hgdprs1057518212
ensemblrs1057518212
geneviewrs1057518212
scholarrs1057518212
googlers1057518212
pharmgkbrs1057518212
gwascentralrs1057518212
openSNPrs1057518212
23andMers1057518212
23andMe allrs1057518212
SNPshotrs1057518212
SNPdbers1057518212
MSV3drs1057518212
GWAS Ctlgrs1057518212
Max Magnitude0
ClinVar
Risk rs1057518212(G;G)
Alt rs1057518212(G;G)
Reference Rs1057518212(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152275834G>C
CLNSRC
CLNACC RCV000412869.1,