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rs794727122

From SNPedia

Orientationplus
Geno Mag Summary
(CCCTT;CCCTT) 0 common in clinvar
Make rs794727122(-;-)
Make rs794727122(-;CCTTC)
Make rs794727122(CCTTC;CCTTC)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position189894296
GeneTP63
is asnp
is mentioned by
dbSNPrs794727122
ebirs794727122
HLIrs794727122
Exacrs794727122
Varsomers794727122
Maprs794727122
PheGenIrs794727122
hapmaprs794727122
1000 genomesrs794727122
hgdprs794727122
ensemblrs794727122
gopubmedrs794727122
geneviewrs794727122
scholarrs794727122
googlers794727122
pharmgkbrs794727122
gwascentralrs794727122
openSNPrs794727122
23andMers794727122
23andMe allrs794727122
SNP Nexus

SNPshotrs794727122
SNPdbers794727122
MSV3drs794727122
GWAS Ctlgrs794727122
Max Magnitude0
ClinVar
Risk rs794727122(;)
Alt rs794727122(;)
Reference rs794727122(CCCTT;CCCTT)
Significance Pathogenic
Disease Limb-mammary syndrome
Variation info
Gene TP63
CLNDBN Limb-mammary syndrome
Reversed 0
HGVS NC_000003.11:g.189612085_189612089delCCTTC
CLNSRC
CLNACC RCV000174740.1,