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rs864309486

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864309486(A;T)
Make rs864309486(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position24777262
GeneGMNN
is asnp
is mentioned by
dbSNPrs864309486
ebirs864309486
HLIrs864309486
Exacrs864309486
Varsomers864309486
Maprs864309486
PheGenIrs864309486
hapmaprs864309486
1000 genomesrs864309486
hgdprs864309486
ensemblrs864309486
gopubmedrs864309486
geneviewrs864309486
scholarrs864309486
googlers864309486
pharmgkbrs864309486
gwascentralrs864309486
openSNPrs864309486
23andMers864309486
23andMe allrs864309486
SNP Nexus

SNPshotrs864309486
SNPdbers864309486
MSV3drs864309486
GWAS Ctlgrs864309486
Max Magnitude0
ClinVar
Risk rs864309486(T;T)
Alt rs864309486(T;T)
Reference rs864309486(A;A)
Significance Pathogenic
Disease Meier-Gorlin syndrome Meier-gorlin syndrome 6
Variation info
Gene GMNN
CLNDBN Meier-Gorlin syndrome Meier-gorlin syndrome 6
Reversed 0
HGVS NC_000006.11:g.24777490A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000202433.1, RCV000208589.1,