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rs115746363

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs115746363(A;A)
Make rs115746363(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152312410
GeneFLG, FLG-AS1
is asnp
is mentioned by
dbSNPrs115746363
dbSNP (old)rs115746363
ClinGenrs115746363
ebirs115746363
HLIrs115746363
Exacrs115746363
Gnomadrs115746363
Varsomers115746363
Maprs115746363
PheGenIrs115746363
Biobankrs115746363
1000 genomesrs115746363
hgdprs115746363
ensemblrs115746363
gopubmedrs115746363
geneviewrs115746363
scholarrs115746363
googlers115746363
pharmgkbrs115746363
gwascentralrs115746363
openSNPrs115746363
23andMers115746363
23andMe allrs115746363
SNPshotrs115746363
SNPdbers115746363
MSV3drs115746363
GWAS Ctlgrs115746363
Max Magnitude0
ClinVar
Risk rs115746363(A;A)
Alt rs115746363(A;A)
Reference Rs115746363(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG FLG-AS1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152284886G>A
CLNSRC
CLNACC RCV000255117.2,