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rs1057518339

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518339(C;G)
Make rs1057518339(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position55259981
GeneTCF4
is asnp
is mentioned by
dbSNPrs1057518339
dbSNP (old)rs1057518339
ClinGenrs1057518339
ebirs1057518339
HLIrs1057518339
Exacrs1057518339
Gnomadrs1057518339
Varsomers1057518339
LitVarrs1057518339
Maprs1057518339
PheGenIrs1057518339
Biobankrs1057518339
1000 genomesrs1057518339
hgdprs1057518339
ensemblrs1057518339
gopubmedrs1057518339
geneviewrs1057518339
scholarrs1057518339
googlers1057518339
pharmgkbrs1057518339
gwascentralrs1057518339
openSNPrs1057518339
23andMers1057518339
23andMe allrs1057518339
SNPshotrs1057518339
SNPdbers1057518339
MSV3drs1057518339
GWAS Ctlgrs1057518339
Max Magnitude0
ClinVar
Risk rs1057518339(G;G)
Alt rs1057518339(G;G)
Reference Rs1057518339(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene TCF4
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.52927212G>C
CLNSRC
CLNACC RCV000413573.1,