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rs754242209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs754242209(A;A)
Make rs754242209(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome12
Position52515040
GeneKRT5
is asnp
is mentioned by
dbSNPrs754242209
dbSNP (classic)rs754242209
ClinGenrs754242209
ebirs754242209
HLIrs754242209
Exacrs754242209
Gnomadrs754242209
Varsomers754242209
LitVarrs754242209
Maprs754242209
PheGenIrs754242209
Biobankrs754242209
1000 genomesrs754242209
hgdprs754242209
ensemblrs754242209
geneviewrs754242209
scholarrs754242209
googlers754242209
pharmgkbrs754242209
gwascentralrs754242209
openSNPrs754242209
23andMers754242209
23andMe allrs754242209
SNPshotrs754242209
SNPdbers754242209
MSV3drs754242209
GWAS Ctlgrs754242209
Max Magnitude0
ClinVar
Risk rs754242209(A;A)
Alt rs754242209(A;A)
Reference Rs754242209(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene KRT5
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52908824G>A
CLNSRC
CLNACC RCV000256176.1,