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rs786205126

From SNPedia

Orientationplus
Geno Mag Summary
(TCT;TCT) 0 common in clinvar
Make rs786205126(-;-)
Make rs786205126(-;CTT)
Make rs786205126(CTT;CTT)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position93809877
GeneTMEM67
is asnp
is mentioned by
dbSNPrs786205126
ebirs786205126
HLIrs786205126
Exacrs786205126
Varsomers786205126
Maprs786205126
PheGenIrs786205126
hapmaprs786205126
1000 genomesrs786205126
hgdprs786205126
ensemblrs786205126
gopubmedrs786205126
geneviewrs786205126
scholarrs786205126
googlers786205126
pharmgkbrs786205126
gwascentralrs786205126
openSNPrs786205126
23andMers786205126
23andMe allrs786205126
SNP Nexus

SNPshotrs786205126
SNPdbers786205126
MSV3drs786205126
GWAS Ctlgrs786205126
Max Magnitude0
ClinVar
Risk rs786205126(;)
Alt rs786205126(;)
Reference rs786205126(TCT;TCT)
Significance Pathogenic
Disease Meckel syndrome type 3
Variation info
Gene TMEM67
CLNDBN Meckel syndrome type 3
Reversed 0
HGVS NC_000008.10:g.94822105_94822107delCTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000049341.4,