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rs151344525

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151344525(C;C)
Make rs151344525(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10404562
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs151344525
ebirs151344525
HLIrs151344525
Exacrs151344525
Varsomers151344525
Maprs151344525
PheGenIrs151344525
hapmaprs151344525
1000 genomesrs151344525
hgdprs151344525
ensemblrs151344525
gopubmedrs151344525
geneviewrs151344525
scholarrs151344525
googlers151344525
pharmgkbrs151344525
gwascentralrs151344525
openSNPrs151344525
23andMers151344525
23andMe allrs151344525
SNP Nexus

SNPshotrs151344525
SNPdbers151344525
MSV3drs151344525
GWAS Ctlgrs151344525
Max Magnitude0
ClinVar
Risk rs151344525(A,C;A,C)
Alt rs151344525(A,C;A,C)
Reference rs151344525(G;G)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10404795C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019536.26,