Have questions? Visit https://www.reddit.com/r/SNPedia

rs199469487

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GCTTTCAA;GCTTTCAA) 0 common in clinvar
Make rs199469487(GCTTTCAA;TGAAAGC)
Make rs199469487(TGAAAGC;TGAAAGC)
ReferenceGRCh38 38.1/141
Chromosome3
Position93905802
GenePROS1
is asnp
is mentioned by
dbSNPrs199469487
ebirs199469487
HLIrs199469487
Exacrs199469487
Varsomers199469487
Maprs199469487
PheGenIrs199469487
hapmaprs199469487
1000 genomesrs199469487
hgdprs199469487
ensemblrs199469487
gopubmedrs199469487
geneviewrs199469487
scholarrs199469487
googlers199469487
pharmgkbrs199469487
gwascentralrs199469487
openSNPrs199469487
23andMers199469487
23andMe allrs199469487
SNP Nexus

SNPshotrs199469487
SNPdbers199469487
MSV3drs199469487
GWAS Ctlgrs199469487
Max Magnitude0
ClinVar
Risk rs199469487(TGAAAGC;TGAAAGC)
Alt rs199469487(TGAAAGC;TGAAAGC)
Reference rs199469487(GCTTTCAA;GCTTTCAA)
Significance Untested
Disease
Variation info
Gene PROS1
CLNDBN OMIM
Reversed 1
HGVS NC_000003.11:g.93624646_93624653delTTGAAAGCinsGCTTTCA
CLNSRC
CLNACC