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rs149484917

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149484917(C;C)
Make rs149484917(C;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152304939
GeneFLG
is asnp
is mentioned by
dbSNPrs149484917
dbSNP (old)rs149484917
ClinGenrs149484917
ebirs149484917
HLIrs149484917
Exacrs149484917
Gnomadrs149484917
Varsomers149484917
Maprs149484917
PheGenIrs149484917
Biobankrs149484917
1000 genomesrs149484917
hgdprs149484917
ensemblrs149484917
gopubmedrs149484917
geneviewrs149484917
scholarrs149484917
googlers149484917
pharmgkbrs149484917
gwascentralrs149484917
openSNPrs149484917
23andMers149484917
23andMe allrs149484917
SNP Nexus

SNPshotrs149484917
SNPdbers149484917
MSV3drs149484917
GWAS Ctlgrs149484917
Max Magnitude0
ClinVar
Risk rs149484917(C;C)
Alt rs149484917(C;C)
Reference Rs149484917(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152277415G>C
CLNSRC
CLNACC RCV000293549.2,