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rs61753245

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61753245(A;A)
Make rs61753245(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position136866718
GenePEX7
is asnp
is mentioned by
dbSNPrs61753245
ebirs61753245
HLIrs61753245
Exacrs61753245
Varsomers61753245
Maprs61753245
PheGenIrs61753245
hapmaprs61753245
1000 genomesrs61753245
hgdprs61753245
ensemblrs61753245
gopubmedrs61753245
geneviewrs61753245
scholarrs61753245
googlers61753245
pharmgkbrs61753245
gwascentralrs61753245
openSNPrs61753245
23andMers61753245
23andMe allrs61753245
SNP Nexus

SNPshotrs61753245
SNPdbers61753245
MSV3drs61753245
GWAS Ctlgrs61753245
Max Magnitude0
ClinVar
Risk rs61753245(A;A)
Alt rs61753245(A;A)
Reference rs61753245(G;G)
Significance Probable-Pathogenic
Disease Rhizomelic chondrodysplasia punctata type 1
Variation info
Gene PEX7
CLNDBN Rhizomelic chondrodysplasia punctata type 1
Reversed 0
HGVS NC_000006.11:g.137187856G>A
CLNSRC
CLNACC RCV000169479.1,