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rs1057519493

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519493(C;T)
Make rs1057519493(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position5583761
GeneNLRP1
is asnp
is mentioned by
dbSNPrs1057519493
dbSNP (classic)rs1057519493
ClinGenrs1057519493
ebirs1057519493
HLIrs1057519493
Exacrs1057519493
Gnomadrs1057519493
Varsomers1057519493
LitVarrs1057519493
Maprs1057519493
PheGenIrs1057519493
Biobankrs1057519493
1000 genomesrs1057519493
hgdprs1057519493
ensemblrs1057519493
geneviewrs1057519493
scholarrs1057519493
googlers1057519493
pharmgkbrs1057519493
gwascentralrs1057519493
openSNPrs1057519493
23andMers1057519493
SNPshotrs1057519493
SNPdbers1057519493
MSV3drs1057519493
GWAS Ctlgrs1057519493
Max Magnitude0
ClinVar
Risk rs1057519493(T;T)
Alt rs1057519493(T;T)
Reference Rs1057519493(C;C)
Significance Pathogenic
Disease Palmoplantar carcinoma not provided
Variation info
Gene NLRP1
CLNDBN Palmoplantar carcinoma, multiple self-healing not provided
Reversed 1
HGVS NC_000017.10:g.5487081G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000416502.1, RCV000479210.1,