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rs1057517973

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Make rs1057517973(-;-)
Make rs1057517973(-;AG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152310881
GeneFLG
is asnp
is mentioned by
dbSNPrs1057517973
dbSNP (old)rs1057517973
ClinGenrs1057517973
ebirs1057517973
HLIrs1057517973
Exacrs1057517973
Gnomadrs1057517973
Varsomers1057517973
Maprs1057517973
PheGenIrs1057517973
Biobankrs1057517973
1000 genomesrs1057517973
hgdprs1057517973
ensemblrs1057517973
gopubmedrs1057517973
geneviewrs1057517973
scholarrs1057517973
googlers1057517973
pharmgkbrs1057517973
gwascentralrs1057517973
openSNPrs1057517973
23andMers1057517973
23andMe allrs1057517973
SNPshotrs1057517973
SNPdbers1057517973
MSV3drs1057517973
GWAS Ctlgrs1057517973
Max Magnitude0
ClinVar
Risk rs1057517973(-;-)
Alt rs1057517973(-;-)
Reference Rs1057517973(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.152283357_152283358delCT
CLNSRC
CLNACC RCV000414010.1,