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rs267607472

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CAA;CAA) 0 common in clinvar
Make rs267607472(-;-)
Make rs267607472(-;CAA)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52451561
GeneKRT6B
is asnp
is mentioned by
dbSNPrs267607472
dbSNP (old)rs267607472
ClinGenrs267607472
ebirs267607472
HLIrs267607472
Exacrs267607472
Gnomadrs267607472
Varsomers267607472
LitVarrs267607472
Maprs267607472
PheGenIrs267607472
Biobankrs267607472
1000 genomesrs267607472
hgdprs267607472
ensemblrs267607472
gopubmedrs267607472
geneviewrs267607472
scholarrs267607472
googlers267607472
pharmgkbrs267607472
gwascentralrs267607472
openSNPrs267607472
23andMers267607472
23andMe allrs267607472
SNPshotrs267607472
SNPdbers267607472
MSV3drs267607472
GWAS Ctlgrs267607472
Max Magnitude0
ClinVar
Risk rs267607472(-;-)
Alt rs267607472(-;-)
Reference Rs267607472(CAA;CAA)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT6B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.52845345_52845347delTTG
CLNSRC
CLNACC RCV000057024.2,