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rs104894610

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894610(G;T)
Make rs104894610(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position56594834
GeneNOG
is asnp
is mentioned by
dbSNPrs104894610
ebirs104894610
HLIrs104894610
Exacrs104894610
Varsomers104894610
Maprs104894610
PheGenIrs104894610
hapmaprs104894610
1000 genomesrs104894610
hgdprs104894610
ensemblrs104894610
gopubmedrs104894610
geneviewrs104894610
scholarrs104894610
googlers104894610
pharmgkbrs104894610
gwascentralrs104894610
openSNPrs104894610
23andMers104894610
23andMe allrs104894610
SNP Nexus

SNPshotrs104894610
SNPdbers104894610
MSV3drs104894610
GWAS Ctlgrs104894610
Max Magnitude0
OMIM602991
Desc
Variant0006
Relatedalso
ClinVar
Risk rs104894610(T;T)
Alt rs104894610(T;T)
Reference rs104894610(G;G)
Significance Pathogenic
Disease Tarsal carpal coalition syndrome
Variation info
Gene NOG
CLNDBN Tarsal carpal coalition syndrome
Reversed 0
HGVS NC_000017.10:g.54672195G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000007084.2,