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rs150597413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150597413(G;T)
Make rs150597413(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position152305146
GeneFLG
is asnp
is mentioned by
dbSNPrs150597413
dbSNP (old)rs150597413
ClinGenrs150597413
ebirs150597413
HLIrs150597413
Exacrs150597413
Gnomadrs150597413
Varsomers150597413
Maprs150597413
PheGenIrs150597413
Biobankrs150597413
1000 genomesrs150597413
hgdprs150597413
ensemblrs150597413
gopubmedrs150597413
geneviewrs150597413
scholarrs150597413
googlers150597413
pharmgkbrs150597413
gwascentralrs150597413
openSNPrs150597413
23andMers150597413
23andMe allrs150597413
SNP Nexus

SNPshotrs150597413
SNPdbers150597413
MSV3drs150597413
GWAS Ctlgrs150597413
Max Magnitude0
ClinVar
Risk rs150597413(A;A) rs150597413(T;T)
Alt rs150597413(A;A) rs150597413(T;T)
Reference Rs150597413(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FLG
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.152277622G>T
CLNSRC
CLNACC RCV000255466.1,