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rs767222404

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs767222404(A;A)
Make rs767222404(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position2993574
GeneTLE6
is asnp
is mentioned by
dbSNPrs767222404
ebirs767222404
HLIrs767222404
Exacrs767222404
Varsomers767222404
Maprs767222404
PheGenIrs767222404
hapmaprs767222404
1000 genomesrs767222404
hgdprs767222404
ensemblrs767222404
gopubmedrs767222404
geneviewrs767222404
scholarrs767222404
googlers767222404
pharmgkbrs767222404
gwascentralrs767222404
openSNPrs767222404
23andMers767222404
23andMe allrs767222404
SNP Nexus

SNPshotrs767222404
SNPdbers767222404
MSV3drs767222404
GWAS Ctlgrs767222404
Max Magnitude0
ClinVar
Risk rs767222404(A,G;A,G)
Alt rs767222404(A,G;A,G)
Reference rs767222404(C;C)
Significance Pathogenic
Disease Preimplantation embryonic lethality
Variation info
Gene TLE6
CLNDBN Preimplantation embryonic lethality
Reversed 0
HGVS NC_000019.9:g.2993572C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000207476.2,