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rs4636294

From SNPedia

Orientationplus
Stabilizedplus
Make rs4636294(A;A)
Make rs4636294(A;G)
Make rs4636294(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position21747804
is asnp
is mentioned by
dbSNPrs4636294
ebirs4636294
HLIrs4636294
Exacrs4636294
Varsomers4636294
Maprs4636294
PheGenIrs4636294
hapmaprs4636294
1000 genomesrs4636294
hgdprs4636294
ensemblrs4636294
gopubmedrs4636294
geneviewrs4636294
scholarrs4636294
googlers4636294
pharmgkbrs4636294
gwascentralrs4636294
openSNPrs4636294
23andMers4636294
23andMe allrs4636294
SNP Nexus

SNPshotrs4636294
SNPdbers4636294
MSV3drs4636294
GWAS Ctlgrs4636294
GMAF0.3751
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19578365OA-icon.png]
Trait Cutaneous nevi
Title Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi
Risk Allele A
P-val 3E-15
Odds Ratio 0.20 [0.13-0.27] increase in log nevus count
OMIM155601
Desc
Variant
Relatedalso
OMIM162900
Desc
Variant
Relatedalso
[PMID 19578364OA-icon.png] Genome-wide association study identifies three loci associated with melanoma risk.

[PMID 19686382OA-icon.png] Genome-wide associations studies for melanoma and nevi.


GET Evidence
rs4636294
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.703125
summary