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rs121909574

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121909574(A;G)
Make rs121909574(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10404509
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs121909574
ebirs121909574
HLIrs121909574
Exacrs121909574
Varsomers121909574
Maprs121909574
PheGenIrs121909574
hapmaprs121909574
1000 genomesrs121909574
hgdprs121909574
ensemblrs121909574
gopubmedrs121909574
geneviewrs121909574
scholarrs121909574
googlers121909574
pharmgkbrs121909574
gwascentralrs121909574
openSNPrs121909574
23andMers121909574
23andMe allrs121909574
SNP Nexus

SNPshotrs121909574
SNPdbers121909574
MSV3drs121909574
GWAS Ctlgrs121909574
Max Magnitude0
OMIM107580
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909574(C,G;C,G)
Alt rs121909574(C,G;C,G)
Reference rs121909574(A;A)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10404742T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000019530.25,