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rs1057518148

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518148(C;T)
Make rs1057518148(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152309656
GeneFLG
is asnp
is mentioned by
dbSNPrs1057518148
dbSNP (old)rs1057518148
ClinGenrs1057518148
ebirs1057518148
HLIrs1057518148
Exacrs1057518148
Gnomadrs1057518148
Varsomers1057518148
Maprs1057518148
PheGenIrs1057518148
Biobankrs1057518148
1000 genomesrs1057518148
hgdprs1057518148
ensemblrs1057518148
gopubmedrs1057518148
geneviewrs1057518148
scholarrs1057518148
googlers1057518148
pharmgkbrs1057518148
gwascentralrs1057518148
openSNPrs1057518148
23andMers1057518148
23andMe allrs1057518148
SNP Nexus

SNPshotrs1057518148
SNPdbers1057518148
MSV3drs1057518148
GWAS Ctlgrs1057518148
Max Magnitude0
ClinVar
Risk rs1057518148(T;T)
Alt rs1057518148(T;T)
Reference Rs1057518148(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152282132G>A
CLNSRC
CLNACC RCV000414080.1,