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rs151344526

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151344526(A;A)
Make rs151344526(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10404548
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs151344526
ebirs151344526
HLIrs151344526
Exacrs151344526
Varsomers151344526
Maprs151344526
PheGenIrs151344526
hapmaprs151344526
1000 genomesrs151344526
hgdprs151344526
ensemblrs151344526
gopubmedrs151344526
geneviewrs151344526
scholarrs151344526
googlers151344526
pharmgkbrs151344526
gwascentralrs151344526
openSNPrs151344526
23andMers151344526
23andMe allrs151344526
SNP Nexus

SNPshotrs151344526
SNPdbers151344526
MSV3drs151344526
GWAS Ctlgrs151344526
Max Magnitude0
ClinVar
Risk rs151344526(A;A)
Alt rs151344526(A;A)
Reference rs151344526(G;G)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10404781C>T
CLNSRC
CLNACC