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rs776975632

From SNPedia

Orientationplus
Stabilizedplus
Make rs776975632(C;C)
Make rs776975632(C;T)
Make rs776975632(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position68828254
GeneCDH1
is asnp
is mentioned by
dbSNPrs776975632
dbSNP (old)rs776975632
ClinGenrs776975632
ebirs776975632
HLIrs776975632
Exacrs776975632
Gnomadrs776975632
Varsomers776975632
Maprs776975632
PheGenIrs776975632
Biobankrs776975632
1000 genomesrs776975632
hgdprs776975632
ensemblrs776975632
gopubmedrs776975632
geneviewrs776975632
scholarrs776975632
googlers776975632
pharmgkbrs776975632
gwascentralrs776975632
openSNPrs776975632
23andMers776975632
23andMe allrs776975632
SNP Nexus

SNPshotrs776975632
SNPdbers776975632
MSV3drs776975632
GWAS Ctlgrs776975632
Max Magnitude
ClinVar
Risk rs776975632(T;T)
Alt rs776975632(T;T)
Reference rs776975632(C;C)
Significance Unknown
Disease not specified
Variation info
Gene CDH1
CLNDBN not specified
Reversed 0
HGVS NC_000016.9:g.68862157C>T
CLNSRC
CLNACC RCV000479819.1,