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rs1057517915

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517915(G;T)
Make rs1057517915(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position140754202
GeneBRAF
is asnp
is mentioned by
dbSNPrs1057517915
dbSNP (old)rs1057517915
ClinGenrs1057517915
ebirs1057517915
HLIrs1057517915
Exacrs1057517915
Gnomadrs1057517915
Varsomers1057517915
Maprs1057517915
PheGenIrs1057517915
Biobankrs1057517915
1000 genomesrs1057517915
hgdprs1057517915
ensemblrs1057517915
gopubmedrs1057517915
geneviewrs1057517915
scholarrs1057517915
googlers1057517915
pharmgkbrs1057517915
gwascentralrs1057517915
openSNPrs1057517915
23andMers1057517915
23andMe allrs1057517915
SNPshotrs1057517915
SNPdbers1057517915
MSV3drs1057517915
GWAS Ctlgrs1057517915
Max Magnitude0
ClinVar
Risk rs1057517915(T;T)
Alt rs1057517915(T;T)
Reference Rs1057517915(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BRAF
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.140454002C>A
CLNSRC
CLNACC RCV000413723.1,