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rs765196598

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs765196598(A;A)
Make rs765196598(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position196247479
GenePCYT1A
is asnp
is mentioned by
dbSNPrs765196598
dbSNP (classic)rs765196598
ClinGenrs765196598
ebirs765196598
HLIrs765196598
Exacrs765196598
Gnomadrs765196598
Varsomers765196598
LitVarrs765196598
Maprs765196598
PheGenIrs765196598
Biobankrs765196598
1000 genomesrs765196598
hgdprs765196598
ensemblrs765196598
geneviewrs765196598
scholarrs765196598
googlers765196598
pharmgkbrs765196598
gwascentralrs765196598
openSNPrs765196598
23andMers765196598
SNPshotrs765196598
SNPdbers765196598
MSV3drs765196598
GWAS Ctlgrs765196598
Max Magnitude0
ClinVar
Risk rs765196598(A;A)
Alt rs765196598(A;A)
Reference Rs765196598(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCYT1A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.195974350G>A
CLNSRC
CLNACC RCV000412999.1,