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rs762679102

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs762679102(A;T)
Make rs762679102(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome15
Position100501807
GeneCERS3
is asnp
is mentioned by
dbSNPrs762679102
ebirs762679102
HLIrs762679102
Exacrs762679102
Varsomers762679102
Maprs762679102
PheGenIrs762679102
hapmaprs762679102
1000 genomesrs762679102
hgdprs762679102
ensemblrs762679102
gopubmedrs762679102
geneviewrs762679102
scholarrs762679102
googlers762679102
pharmgkbrs762679102
gwascentralrs762679102
openSNPrs762679102
23andMers762679102
23andMe allrs762679102
SNP Nexus

SNPshotrs762679102
SNPdbers762679102
MSV3drs762679102
GWAS Ctlgrs762679102
Max Magnitude0
ClinVar
Risk rs762679102(T;T)
Alt rs762679102(T;T)
Reference rs762679102(A;A)
Significance Pathogenic
Disease Autosomal recessive congenital ichthyosis 9
Variation info
Gene CERS3
CLNDBN Autosomal recessive congenital ichthyosis 9
Reversed 0
HGVS NC_000015.9:g.101042012A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000054808.2,