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rs267608252

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608252(C;T)
Make rs267608252(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position136822621
GenePEX7
is asnp
is mentioned by
dbSNPrs267608252
ebirs267608252
HLIrs267608252
Exacrs267608252
Varsomers267608252
Maprs267608252
PheGenIrs267608252
hapmaprs267608252
1000 genomesrs267608252
hgdprs267608252
ensemblrs267608252
gopubmedrs267608252
geneviewrs267608252
scholarrs267608252
googlers267608252
pharmgkbrs267608252
gwascentralrs267608252
openSNPrs267608252
23andMers267608252
23andMe allrs267608252
SNP Nexus

SNPshotrs267608252
SNPdbers267608252
MSV3drs267608252
GWAS Ctlgrs267608252
Max Magnitude0
ClinVar
Risk rs267608252(T;T)
Alt rs267608252(T;T)
Reference rs267608252(C;C)
Significance Pathogenic
Disease Phytanic acid storage disease
Variation info
Gene PEX7
CLNDBN Phytanic acid storage disease
Reversed 0
HGVS NC_000006.11:g.137143759C>T
CLNSRC ClinVar GeneReviews
CLNACC RCV000032114.1,