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rs587779765

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779765(A;C)
Make rs587779765(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position24255388
GeneTGM1
is asnp
is mentioned by
dbSNPrs587779765
ebirs587779765
HLIrs587779765
Exacrs587779765
Varsomers587779765
Maprs587779765
PheGenIrs587779765
hapmaprs587779765
1000 genomesrs587779765
hgdprs587779765
ensemblrs587779765
gopubmedrs587779765
geneviewrs587779765
scholarrs587779765
googlers587779765
pharmgkbrs587779765
gwascentralrs587779765
openSNPrs587779765
23andMers587779765
23andMe allrs587779765
SNP Nexus

SNPshotrs587779765
SNPdbers587779765
MSV3drs587779765
GWAS Ctlgrs587779765
Max Magnitude0
ClinVar
Risk rs587779765(C;C)
Alt rs587779765(C;C)
Reference rs587779765(A;A)
Significance Pathogenic
Disease Lamellar ichthyosis
Variation info
Gene TGM1
CLNDBN Lamellar ichthyosis
Reversed 1
HGVS NC_000014.8:g.24724594T>G
CLNSRC
CLNACC RCV000114933.1,