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rs1057519695

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs1057519695(AA;TG)
Make rs1057519695(TG;TG)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position114713907
GeneNRAS
is asnp
is mentioned by
dbSNPrs1057519695
dbSNP (old)rs1057519695
ClinGenrs1057519695
ebirs1057519695
HLIrs1057519695
Exacrs1057519695
Gnomadrs1057519695
Varsomers1057519695
Maprs1057519695
PheGenIrs1057519695
Biobankrs1057519695
1000 genomesrs1057519695
hgdprs1057519695
ensemblrs1057519695
gopubmedrs1057519695
geneviewrs1057519695
scholarrs1057519695
googlers1057519695
pharmgkbrs1057519695
gwascentralrs1057519695
openSNPrs1057519695
23andMers1057519695
23andMe allrs1057519695
SNPshotrs1057519695
SNPdbers1057519695
MSV3drs1057519695
GWAS Ctlgrs1057519695
Max Magnitude0
ClinVar
Risk rs1057519695(GG;GG) rs1057519695(TG;TG)
Alt rs1057519695(GG;GG) rs1057519695(TG;TG)
Reference Rs1057519695(AA;AA)
Significance Pathogenic
Disease Malignant melanoma
Variation info
Gene NRAS
CLNDBN Malignant melanoma
Reversed 1
HGVS NC_000001.10:g.115256528_115256529delTTinsCA; NC_000001.10:g.115256528_115256529delTTinsCC
CLNSRC
CLNACC RCV000443704.1, RCV000425830.1,