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rs786205618

From SNPedia

Orientationminus
Geno Mag Summary
(CTT;CTT) 0 common in clinvar
Make rs786205618(-;-)
Make rs786205618(-;CTT)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position124923384
GeneHEPACAM
is asnp
is mentioned by
dbSNPrs786205618
ebirs786205618
HLIrs786205618
Exacrs786205618
Varsomers786205618
Maprs786205618
PheGenIrs786205618
hapmaprs786205618
1000 genomesrs786205618
hgdprs786205618
ensemblrs786205618
gopubmedrs786205618
geneviewrs786205618
scholarrs786205618
googlers786205618
pharmgkbrs786205618
gwascentralrs786205618
openSNPrs786205618
23andMers786205618
23andMe allrs786205618
SNP Nexus

SNPshotrs786205618
SNPdbers786205618
MSV3drs786205618
GWAS Ctlgrs786205618
Max Magnitude0
ClinVar
Risk rs786205618(;)
Alt rs786205618(;)
Reference rs786205618(CTT;CTT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HEPACAM
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.124793280_124793282delAAG
CLNSRC
CLNACC RCV000171466.1,