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rs1057519834

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs1057519834(AG;AG)
Make rs1057519834(AG;CA)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position114713908
GeneNRAS
is asnp
is mentioned by
dbSNPrs1057519834
dbSNP (classic)rs1057519834
ClinGenrs1057519834
ebirs1057519834
HLIrs1057519834
Exacrs1057519834
Gnomadrs1057519834
Varsomers1057519834
LitVarrs1057519834
Maprs1057519834
PheGenIrs1057519834
Biobankrs1057519834
1000 genomesrs1057519834
hgdprs1057519834
ensemblrs1057519834
geneviewrs1057519834
scholarrs1057519834
googlers1057519834
pharmgkbrs1057519834
gwascentralrs1057519834
openSNPrs1057519834
23andMers1057519834
23andMe allrs1057519834
SNPshotrs1057519834
SNPdbers1057519834
MSV3drs1057519834
GWAS Ctlgrs1057519834
Max Magnitude0
ClinVar
Risk rs1057519834(AG;AG)
Alt rs1057519834(AG;AG)
Reference Rs1057519834(CA;CA)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene NRAS
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000001.10:g.115256529_115256530delTGinsCT
CLNSRC
CLNACC RCV000426087.1,