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rs754645487

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754645487(A;A)
Make rs754645487(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position122462103
GeneHTRA1, LOC105378525
is asnp
is mentioned by
dbSNPrs754645487
dbSNP (classic)rs754645487
ClinGenrs754645487
ebirs754645487
HLIrs754645487
Exacrs754645487
Gnomadrs754645487
Varsomers754645487
LitVarrs754645487
Maprs754645487
PheGenIrs754645487
Biobankrs754645487
1000 genomesrs754645487
hgdprs754645487
ensemblrs754645487
geneviewrs754645487
scholarrs754645487
googlers754645487
pharmgkbrs754645487
gwascentralrs754645487
openSNPrs754645487
23andMers754645487
23andMe allrs754645487
SNPshotrs754645487
SNPdbers754645487
MSV3drs754645487
GWAS Ctlgrs754645487
Max Magnitude0
ClinVar
Risk rs754645487(A;A) rs754645487(T;T)
Alt rs754645487(A;A) rs754645487(T;T)
Reference Rs754645487(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HTRA1
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.124221619C>T
CLNSRC
CLNACC RCV000487710.1,