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rs267607108

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267607108(A;A)
Make rs267607108(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position10400587
GeneTFAP2A
is asnp
is mentioned by
dbSNPrs267607108
ebirs267607108
HLIrs267607108
Exacrs267607108
Varsomers267607108
Maprs267607108
PheGenIrs267607108
hapmaprs267607108
1000 genomesrs267607108
hgdprs267607108
ensemblrs267607108
gopubmedrs267607108
geneviewrs267607108
scholarrs267607108
googlers267607108
pharmgkbrs267607108
gwascentralrs267607108
openSNPrs267607108
23andMers267607108
23andMe allrs267607108
SNP Nexus

SNPshotrs267607108
SNPdbers267607108
MSV3drs267607108
GWAS Ctlgrs267607108
Max Magnitude0
ClinVar
Risk rs267607108(A;A)
Alt rs267607108(A;A)
Reference rs267607108(G;G)
Significance Pathogenic
Disease Branchiooculofacial syndrome
Variation info
Gene TFAP2A
CLNDBN Branchiooculofacial syndrome
Reversed 1
HGVS NC_000006.11:g.10400820C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000019535.23,