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rs765371196

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs765371196(C;C)
Make rs765371196(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position95461864
GeneLOC100507346, PTCH1
is asnp
is mentioned by
dbSNPrs765371196
ebirs765371196
HLIrs765371196
Exacrs765371196
Varsomers765371196
Maprs765371196
PheGenIrs765371196
hapmaprs765371196
1000 genomesrs765371196
hgdprs765371196
ensemblrs765371196
gopubmedrs765371196
geneviewrs765371196
scholarrs765371196
googlers765371196
pharmgkbrs765371196
gwascentralrs765371196
openSNPrs765371196
23andMers765371196
23andMe allrs765371196
SNP Nexus

SNPshotrs765371196
SNPdbers765371196
MSV3drs765371196
GWAS Ctlgrs765371196
Max Magnitude0
ClinVar
Risk rs765371196(C;C)
Alt rs765371196(C;C)
Reference rs765371196(T;T)
Significance Probable-Pathogenic
Disease Peters anomaly
Variation info
Gene LOC100507346 PTCH1
CLNDBN Peters anomaly
Reversed 0
HGVS NC_000009.11:g.98224146T>C
CLNSRC
CLNACC RCV000207421.1,