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rs876661107

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661107(A;A)
Make rs876661107(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68808504
GeneCDH1
is asnp
is mentioned by
dbSNPrs876661107
ebirs876661107
HLIrs876661107
Exacrs876661107
Varsomers876661107
Maprs876661107
PheGenIrs876661107
hapmaprs876661107
1000 genomesrs876661107
hgdprs876661107
ensemblrs876661107
gopubmedrs876661107
geneviewrs876661107
scholarrs876661107
googlers876661107
pharmgkbrs876661107
gwascentralrs876661107
openSNPrs876661107
23andMers876661107
23andMe allrs876661107
SNP Nexus

SNPshotrs876661107
SNPdbers876661107
MSV3drs876661107
GWAS Ctlgrs876661107
Max Magnitude0
ClinVar
Risk rs876661107(A;A)
Alt rs876661107(A;A)
Reference rs876661107(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CDH1
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.68842407G>A
CLNSRC
CLNACC RCV000218005.1,