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rs151344527

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151344527(A;A)
Make rs151344527(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10404520
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs151344527
ebirs151344527
HLIrs151344527
Exacrs151344527
Varsomers151344527
Maprs151344527
PheGenIrs151344527
hapmaprs151344527
1000 genomesrs151344527
hgdprs151344527
ensemblrs151344527
gopubmedrs151344527
geneviewrs151344527
scholarrs151344527
googlers151344527
pharmgkbrs151344527
gwascentralrs151344527
openSNPrs151344527
23andMers151344527
23andMe allrs151344527
SNP Nexus

SNPshotrs151344527
SNPdbers151344527
MSV3drs151344527
GWAS Ctlgrs151344527
Max Magnitude0
ClinVar
Risk rs151344527(A;A)
Alt rs151344527(A;A)
Reference rs151344527(G;G)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10404753C>T
CLNSRC
CLNACC