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rs749672064

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs749672064(C;T)
Make rs749672064(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position128588887
GeneSPTAN1
is asnp
is mentioned by
dbSNPrs749672064
ebirs749672064
HLIrs749672064
Exacrs749672064
Varsomers749672064
Maprs749672064
PheGenIrs749672064
hapmaprs749672064
1000 genomesrs749672064
hgdprs749672064
ensemblrs749672064
gopubmedrs749672064
geneviewrs749672064
scholarrs749672064
googlers749672064
pharmgkbrs749672064
gwascentralrs749672064
openSNPrs749672064
23andMers749672064
23andMe allrs749672064
SNP Nexus

SNPshotrs749672064
SNPdbers749672064
MSV3drs749672064
GWAS Ctlgrs749672064
Max Magnitude0
ClinVar
Risk rs749672064(T;T)
Alt rs749672064(T;T)
Reference rs749672064(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SPTAN1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.131351166C>T
CLNSRC
CLNACC RCV000189548.1,