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rs151344524

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151344524(C;G)
Make rs151344524(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10404563
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs151344524
ebirs151344524
HLIrs151344524
Exacrs151344524
Varsomers151344524
Maprs151344524
PheGenIrs151344524
hapmaprs151344524
1000 genomesrs151344524
hgdprs151344524
ensemblrs151344524
gopubmedrs151344524
geneviewrs151344524
scholarrs151344524
googlers151344524
pharmgkbrs151344524
gwascentralrs151344524
openSNPrs151344524
23andMers151344524
23andMe allrs151344524
SNP Nexus

SNPshotrs151344524
SNPdbers151344524
MSV3drs151344524
GWAS Ctlgrs151344524
Max Magnitude0
ClinVar
Risk rs151344524(G;G)
Alt rs151344524(G;G)
Reference rs151344524(C;C)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10404796G>C
CLNSRC
CLNACC