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rs730881672

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730881672(-;-)
Make rs730881672(-;GGC)
Make rs730881672(GGC;GGC)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21974781
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs730881672
ebirs730881672
HLIrs730881672
Exacrs730881672
Varsomers730881672
Maprs730881672
PheGenIrs730881672
hapmaprs730881672
1000 genomesrs730881672
hgdprs730881672
ensemblrs730881672
gopubmedrs730881672
geneviewrs730881672
scholarrs730881672
googlers730881672
pharmgkbrs730881672
gwascentralrs730881672
openSNPrs730881672
23andMers730881672
23andMe allrs730881672
SNP Nexus

SNPshotrs730881672
SNPdbers730881672
MSV3drs730881672
GWAS Ctlgrs730881672
Max Magnitude0
ClinVar
Risk rs730881672(GGC;GGC)
Alt rs730881672(GGC;GGC)
Reference rs730881672(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21974780_21974781insGCC
CLNSRC
CLNACC RCV000160402.1,