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rs796053427

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGGGGCAGAGTGTC;AGGGGCAGAGTGTC) 0 common in clinvar
Make rs796053427(-;-)
Make rs796053427(-;AGGGGCAGAGTGTC)
ReferenceGRCh38.p2 38.2/146
Chromosome18
Position55232640
GeneTCF4
is asnp
is mentioned by
dbSNPrs796053427
ClinGenrs796053427
ebirs796053427
HLIrs796053427
Exacrs796053427
Varsomers796053427
Maprs796053427
PheGenIrs796053427
hapmaprs796053427
1000 genomesrs796053427
hgdprs796053427
ensemblrs796053427
gopubmedrs796053427
geneviewrs796053427
scholarrs796053427
googlers796053427
pharmgkbrs796053427
gwascentralrs796053427
openSNPrs796053427
23andMers796053427
23andMe allrs796053427
SNP Nexus

SNPshotrs796053427
SNPdbers796053427
MSV3drs796053427
GWAS Ctlgrs796053427
Max Magnitude0
ClinVar
Risk rs796053427(-;-)
Alt rs796053427(-;-)
Reference Rs796053427(AGGGGCAGAGTGTC;AGGGGCAGAGTGTC)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52899871_52899884delGACACTCTGCCCCT
CLNSRC
CLNACC RCV000189732.1,