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rs769896492

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs769896492(A;A)
Make rs769896492(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position42966813
GenePEX6
is asnp
is mentioned by
dbSNPrs769896492
ebirs769896492
HLIrs769896492
Exacrs769896492
Varsomers769896492
Maprs769896492
PheGenIrs769896492
hapmaprs769896492
1000 genomesrs769896492
hgdprs769896492
ensemblrs769896492
gopubmedrs769896492
geneviewrs769896492
scholarrs769896492
googlers769896492
pharmgkbrs769896492
gwascentralrs769896492
openSNPrs769896492
23andMers769896492
23andMe allrs769896492
SNP Nexus

SNPshotrs769896492
SNPdbers769896492
MSV3drs769896492
GWAS Ctlgrs769896492
Max Magnitude0
ClinVar
Risk rs769896492(A;A)
Alt rs769896492(A;A)
Reference rs769896492(G;G)
Significance Pathogenic
Disease Heimler syndrome 2
Variation info
Gene PEX6
CLNDBN Heimler syndrome 2
Reversed 0
HGVS NC_000006.11:g.42934551G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000201306.2,