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rs1057519735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519735(A;C)
Make rs1057519735(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position66490577
GeneMAP2K1, SNAPC5
is asnp
is mentioned by
dbSNPrs1057519735
dbSNP (classic)rs1057519735
ClinGenrs1057519735
ebirs1057519735
HLIrs1057519735
Exacrs1057519735
Gnomadrs1057519735
Varsomers1057519735
LitVarrs1057519735
Maprs1057519735
PheGenIrs1057519735
Biobankrs1057519735
1000 genomesrs1057519735
hgdprs1057519735
ensemblrs1057519735
geneviewrs1057519735
scholarrs1057519735
googlers1057519735
pharmgkbrs1057519735
gwascentralrs1057519735
openSNPrs1057519735
23andMers1057519735
SNPshotrs1057519735
SNPdbers1057519735
MSV3drs1057519735
GWAS Ctlgrs1057519735
Max Magnitude0
ClinVar
Risk rs1057519735(C;C)
Alt rs1057519735(C;C)
Reference Rs1057519735(A;A)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene MAP2K1 SNAPC5
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000015.9:g.66782915A>C
CLNSRC
CLNACC RCV000441191.1,