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rs750529207

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs750529207(A;A)
Make rs750529207(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position149028147
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs750529207
dbSNP (classic)rs750529207
ClinGenrs750529207
ebirs750529207
HLIrs750529207
Exacrs750529207
Gnomadrs750529207
Varsomers750529207
LitVarrs750529207
Maprs750529207
PheGenIrs750529207
Biobankrs750529207
1000 genomesrs750529207
hgdprs750529207
ensemblrs750529207
geneviewrs750529207
scholarrs750529207
googlers750529207
pharmgkbrs750529207
gwascentralrs750529207
openSNPrs750529207
23andMers750529207
SNPshotrs750529207
SNPdbers750529207
MSV3drs750529207
GWAS Ctlgrs750529207
Max Magnitude0
ClinVar
Risk rs750529207(A;A)
Alt rs750529207(A;A)
Reference Rs750529207(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.148407710G>A
CLNSRC
CLNACC RCV000484690.1,