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rs201356558

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201356558(A;A)
Make rs201356558(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152304661
GeneFLG
is asnp
is mentioned by
dbSNPrs201356558
dbSNP (classic)rs201356558
ClinGenrs201356558
ebirs201356558
HLIrs201356558
Exacrs201356558
Gnomadrs201356558
Varsomers201356558
LitVarrs201356558
Maprs201356558
PheGenIrs201356558
Biobankrs201356558
1000 genomesrs201356558
hgdprs201356558
ensemblrs201356558
geneviewrs201356558
scholarrs201356558
googlers201356558
pharmgkbrs201356558
gwascentralrs201356558
openSNPrs201356558
23andMers201356558
23andMe allrs201356558
SNPshotrs201356558
SNPdbers201356558
MSV3drs201356558
GWAS Ctlgrs201356558
Max Magnitude0
ClinVar
Risk rs201356558(A;A) rs201356558(C;C)
Alt rs201356558(A;A) rs201356558(C;C)
Reference Rs201356558(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152277137G>A
CLNSRC
CLNACC RCV000255606.1,