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rs776347334

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs776347334(C;T)
Make rs776347334(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position211430974
GeneERBB4
is asnp
is mentioned by
dbSNPrs776347334
dbSNP (old)rs776347334
ClinGenrs776347334
ebirs776347334
HLIrs776347334
Exacrs776347334
Gnomadrs776347334
Varsomers776347334
Maprs776347334
PheGenIrs776347334
Biobankrs776347334
1000 genomesrs776347334
hgdprs776347334
ensemblrs776347334
gopubmedrs776347334
geneviewrs776347334
scholarrs776347334
googlers776347334
pharmgkbrs776347334
gwascentralrs776347334
openSNPrs776347334
23andMers776347334
23andMe allrs776347334
SNP Nexus

SNPshotrs776347334
SNPdbers776347334
MSV3drs776347334
GWAS Ctlgrs776347334
Max Magnitude0
ClinVar
Risk rs776347334(T;T)
Alt rs776347334(T;T)
Reference Rs776347334(C;C)
Significance Probable-Pathogenic
Disease Malignant melanoma
Variation info
Gene ERBB4
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000002.11:g.212295699C>T
CLNSRC
CLNACC RCV000444455.1,