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rs754812742

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754812742(A;A)
Make rs754812742(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position152310981
GeneFLG
is asnp
is mentioned by
dbSNPrs754812742
dbSNP (old)rs754812742
ClinGenrs754812742
ebirs754812742
HLIrs754812742
Exacrs754812742
Gnomadrs754812742
Varsomers754812742
Maprs754812742
PheGenIrs754812742
Biobankrs754812742
1000 genomesrs754812742
hgdprs754812742
ensemblrs754812742
gopubmedrs754812742
geneviewrs754812742
scholarrs754812742
googlers754812742
pharmgkbrs754812742
gwascentralrs754812742
openSNPrs754812742
23andMers754812742
23andMe allrs754812742
SNP Nexus

SNPshotrs754812742
SNPdbers754812742
MSV3drs754812742
GWAS Ctlgrs754812742
Max Magnitude0
ClinVar
Risk rs754812742(A;A) rs754812742(T;T)
Alt rs754812742(A;A) rs754812742(T;T)
Reference Rs754812742(G;G)
Significance Pathogenic
Disease Ichthyosis vulgaris
Variation info
Gene FLG
CLNDBN Ichthyosis vulgaris
Reversed 0
HGVS NC_000001.10:g.152283457G>T
CLNSRC
CLNACC RCV000490412.1,