Have questions? Visit https://www.reddit.com/r/SNPedia

rs587776996

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776996(A;A)
Make rs587776996(A;C)
ReferenceGRCh38 38.1/142
Chromosome15
Position100476085
GeneCERS3
is asnp
is mentioned by
dbSNPrs587776996
ebirs587776996
HLIrs587776996
Exacrs587776996
Varsomers587776996
Maprs587776996
PheGenIrs587776996
hapmaprs587776996
1000 genomesrs587776996
hgdprs587776996
ensemblrs587776996
gopubmedrs587776996
geneviewrs587776996
scholarrs587776996
googlers587776996
pharmgkbrs587776996
gwascentralrs587776996
openSNPrs587776996
23andMers587776996
23andMe allrs587776996
SNP Nexus

SNPshotrs587776996
SNPdbers587776996
MSV3drs587776996
GWAS Ctlgrs587776996
Max Magnitude0
ClinVar
Risk rs587776996(A,C;A,C)
Alt rs587776996(A,C;A,C)
Reference rs587776996(G;G)
Significance Pathogenic
Disease Autosomal recessive congenital ichthyosis 9
Variation info
Gene CERS3
CLNDBN Autosomal recessive congenital ichthyosis 9
Reversed 1
HGVS NC_000015.9:g.101016290C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000049259.2,