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rs78838117

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs78838117(A;A)
Make rs78838117(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome11
Position2909210
GeneSLC22A18
is asnp
is mentioned by
dbSNPrs78838117
ebirs78838117
HLIrs78838117
Exacrs78838117
Varsomers78838117
Maprs78838117
PheGenIrs78838117
hapmaprs78838117
1000 genomesrs78838117
hgdprs78838117
ensemblrs78838117
gopubmedrs78838117
geneviewrs78838117
scholarrs78838117
googlers78838117
pharmgkbrs78838117
gwascentralrs78838117
openSNPrs78838117
23andMers78838117
23andMe allrs78838117
SNP Nexus

SNPshotrs78838117
SNPdbers78838117
MSV3drs78838117
GWAS Ctlgrs78838117
Max Magnitude0
ClinVar
Risk rs78838117(A;A)
Alt rs78838117(A;A)
Reference rs78838117(G;G)
Significance Pathogenic
Disease Rhabdomyosarcoma
Variation info
Gene SLC22A18
CLNDBN Rhabdomyosarcoma, somatic
Reversed 0
HGVS NC_000011.9:g.2930440G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000007392.5,