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rs267599193

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267599193(C;T)
Make rs267599193(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position211713583
GeneERBB4
is asnp
is mentioned by
dbSNPrs267599193
dbSNP (old)rs267599193
ClinGenrs267599193
ebirs267599193
HLIrs267599193
Exacrs267599193
Gnomadrs267599193
Varsomers267599193
Maprs267599193
PheGenIrs267599193
Biobankrs267599193
1000 genomesrs267599193
hgdprs267599193
ensemblrs267599193
gopubmedrs267599193
geneviewrs267599193
scholarrs267599193
googlers267599193
pharmgkbrs267599193
gwascentralrs267599193
openSNPrs267599193
23andMers267599193
23andMe allrs267599193
SNP Nexus

SNPshotrs267599193
SNPdbers267599193
MSV3drs267599193
GWAS Ctlgrs267599193
Max Magnitude0
ClinVar
Risk rs267599193(T;T)
Alt rs267599193(T;T)
Reference Rs267599193(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene ERBB4
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000002.11:g.212578308C>T
CLNSRC
CLNACC RCV000435571.1,