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rs149105551

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149105551(C;C)
Make rs149105551(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152309494
GeneFLG
is asnp
is mentioned by
dbSNPrs149105551
dbSNP (classic)rs149105551
ClinGenrs149105551
ebirs149105551
HLIrs149105551
Exacrs149105551
Gnomadrs149105551
Varsomers149105551
LitVarrs149105551
Maprs149105551
PheGenIrs149105551
Biobankrs149105551
1000 genomesrs149105551
hgdprs149105551
ensemblrs149105551
geneviewrs149105551
scholarrs149105551
googlers149105551
pharmgkbrs149105551
gwascentralrs149105551
openSNPrs149105551
23andMers149105551
SNPshotrs149105551
SNPdbers149105551
MSV3drs149105551
GWAS Ctlgrs149105551
Max Magnitude0
ClinVar
Risk rs149105551(A;A) rs149105551(C;C) rs149105551(T;T)
Alt rs149105551(A;A) rs149105551(C;C) rs149105551(T;T)
Reference Rs149105551(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152281970G>A
CLNSRC
CLNACC RCV000484307.1,