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rs150855676

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs150855676(A;A)
Make rs150855676(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position6112171
GeneCHD5
is asnp
is mentioned by
dbSNPrs150855676
ebirs150855676
HLIrs150855676
Exacrs150855676
Varsomers150855676
Maprs150855676
PheGenIrs150855676
hapmaprs150855676
1000 genomesrs150855676
hgdprs150855676
ensemblrs150855676
gopubmedrs150855676
geneviewrs150855676
scholarrs150855676
googlers150855676
pharmgkbrs150855676
gwascentralrs150855676
openSNPrs150855676
23andMers150855676
23andMe allrs150855676
SNP Nexus

SNPshotrs150855676
SNPdbers150855676
MSV3drs150855676
GWAS Ctlgrs150855676
Max Magnitude0
ClinVar
Risk rs150855676(A;A)
Alt rs150855676(A;A)
Reference rs150855676(G;G)
Significance Untested
Disease Malignant melanoma
Variation info
Gene CHD5
CLNDBN Malignant melanoma
Reversed 0
HGVS NC_000001.11:g.6112171G>A
CLNSRC ClinVar
CLNACC RCV000060228.2,


[PMID 21499247OA-icon.png] Exome sequencing identifies GRIN2A as frequently mutated in melanoma.