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rs730882231

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730882231(A;A)
Make rs730882231(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position201629229
GeneTMEM237
is asnp
is mentioned by
dbSNPrs730882231
ebirs730882231
HLIrs730882231
Exacrs730882231
Varsomers730882231
Maprs730882231
PheGenIrs730882231
hapmaprs730882231
1000 genomesrs730882231
hgdprs730882231
ensemblrs730882231
gopubmedrs730882231
geneviewrs730882231
scholarrs730882231
googlers730882231
pharmgkbrs730882231
gwascentralrs730882231
openSNPrs730882231
23andMers730882231
23andMe allrs730882231
SNP Nexus

SNPshotrs730882231
SNPdbers730882231
MSV3drs730882231
GWAS Ctlgrs730882231
Max Magnitude0
ClinVar
Risk rs730882231(A;A)
Alt rs730882231(A;A)
Reference rs730882231(G;G)
Significance Probable-Pathogenic
Disease Meckel-Gruber syndrome
Variation info
Gene TMEM237
CLNDBN Meckel-Gruber syndrome
Reversed 1
HGVS NC_000002.11:g.202493952C>T
CLNSRC
CLNACC RCV000162151.1,