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rs730882233

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730882233(A;G)
Make rs730882233(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position133817543
GeneEXOC4, LOC101928861
is asnp
is mentioned by
dbSNPrs730882233
ebirs730882233
HLIrs730882233
Exacrs730882233
Varsomers730882233
Maprs730882233
PheGenIrs730882233
hapmaprs730882233
1000 genomesrs730882233
hgdprs730882233
ensemblrs730882233
gopubmedrs730882233
geneviewrs730882233
scholarrs730882233
googlers730882233
pharmgkbrs730882233
gwascentralrs730882233
openSNPrs730882233
23andMers730882233
23andMe allrs730882233
SNP Nexus

SNPshotrs730882233
SNPdbers730882233
MSV3drs730882233
GWAS Ctlgrs730882233
Max Magnitude0
ClinVar
Risk rs730882233(G;G)
Alt rs730882233(G;G)
Reference rs730882233(A;A)
Significance Probable-Pathogenic
Disease Meckel-Gruber syndrome
Variation info
Gene LOC101928861 EXOC4
CLNDBN Meckel-Gruber syndrome
Reversed 0
HGVS NC_000007.13:g.133502296A>G
CLNSRC
CLNACC RCV000162153.1,