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rs1057522775

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057522775(C;C)
Make rs1057522775(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position69956457
GeneMITF
is asnp
is mentioned by
dbSNPrs1057522775
dbSNP (old)rs1057522775
ClinGenrs1057522775
ebirs1057522775
HLIrs1057522775
Exacrs1057522775
Gnomadrs1057522775
Varsomers1057522775
Maprs1057522775
PheGenIrs1057522775
Biobankrs1057522775
1000 genomesrs1057522775
hgdprs1057522775
ensemblrs1057522775
gopubmedrs1057522775
geneviewrs1057522775
scholarrs1057522775
googlers1057522775
pharmgkbrs1057522775
gwascentralrs1057522775
openSNPrs1057522775
23andMers1057522775
23andMe allrs1057522775
SNPshotrs1057522775
SNPdbers1057522775
MSV3drs1057522775
GWAS Ctlgrs1057522775
Max Magnitude0
ClinVar
Risk rs1057522775(C;C)
Alt rs1057522775(C;C)
Reference Rs1057522775(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MITF
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.70005608G>C
CLNSRC
CLNACC RCV000424648.1,