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rs200728983

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200728983(C;T)
Make rs200728983(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position149007044
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs200728983
ebirs200728983
HLIrs200728983
Exacrs200728983
Varsomers200728983
Maprs200728983
PheGenIrs200728983
hapmaprs200728983
1000 genomesrs200728983
hgdprs200728983
ensemblrs200728983
gopubmedrs200728983
geneviewrs200728983
scholarrs200728983
googlers200728983
pharmgkbrs200728983
gwascentralrs200728983
openSNPrs200728983
23andMers200728983
23andMe allrs200728983
SNP Nexus

SNPshotrs200728983
SNPdbers200728983
MSV3drs200728983
GWAS Ctlgrs200728983
Max Magnitude0
ClinVar
Risk rs200728983(A,T;A,T)
Alt rs200728983(A,T;A,T)
Reference rs200728983(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.148386607C>A
CLNSRC
CLNACC RCV000236255.1,