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rs749850181

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749850181(A;A)
Make rs749850181(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position149028348
GeneSH3TC2
is asnp
is mentioned by
dbSNPrs749850181
ebirs749850181
HLIrs749850181
Exacrs749850181
Varsomers749850181
Maprs749850181
PheGenIrs749850181
hapmaprs749850181
1000 genomesrs749850181
hgdprs749850181
ensemblrs749850181
gopubmedrs749850181
geneviewrs749850181
scholarrs749850181
googlers749850181
pharmgkbrs749850181
gwascentralrs749850181
openSNPrs749850181
23andMers749850181
23andMe allrs749850181
SNP Nexus

SNPshotrs749850181
SNPdbers749850181
MSV3drs749850181
GWAS Ctlgrs749850181
Max Magnitude0
ClinVar
Risk rs749850181(A;A)
Alt rs749850181(A;A)
Reference rs749850181(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SH3TC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.148407911C>A
CLNSRC
CLNACC RCV000214436.1,