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rs1057519955

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519955(C;T)
Make rs1057519955(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218584682
GeneCNOT9
is asnp
is mentioned by
dbSNPrs1057519955
dbSNP (old)rs1057519955
ClinGenrs1057519955
ebirs1057519955
HLIrs1057519955
Exacrs1057519955
Gnomadrs1057519955
Varsomers1057519955
Maprs1057519955
PheGenIrs1057519955
Biobankrs1057519955
1000 genomesrs1057519955
hgdprs1057519955
ensemblrs1057519955
gopubmedrs1057519955
geneviewrs1057519955
scholarrs1057519955
googlers1057519955
pharmgkbrs1057519955
gwascentralrs1057519955
openSNPrs1057519955
23andMers1057519955
23andMe allrs1057519955
SNPshotrs1057519955
SNPdbers1057519955
MSV3drs1057519955
GWAS Ctlgrs1057519955
Max Magnitude0
ClinVar
Risk rs1057519955(T;T)
Alt rs1057519955(T;T)
Reference Rs1057519955(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin
Variation info
Gene RQCD1 CNOT9
CLNDBN Malignant melanoma of skin
Reversed 0
HGVS NC_000002.11:g.219449405C>T
CLNSRC
CLNACC RCV000439915.1,