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rs730881675

From SNPedia

Orientationminus
Geno Mag Summary
(ACCCGTGCACGACG;ACCCGTGCACGACG) 0 common in clinvar
Make rs730881675(-;-)
Make rs730881675(-;ACCCGTGCACGACG)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position21971106
GeneCDKN2A
is asnp
is mentioned by
dbSNPrs730881675
ebirs730881675
HLIrs730881675
Exacrs730881675
Varsomers730881675
Maprs730881675
PheGenIrs730881675
hapmaprs730881675
1000 genomesrs730881675
hgdprs730881675
ensemblrs730881675
gopubmedrs730881675
geneviewrs730881675
scholarrs730881675
googlers730881675
pharmgkbrs730881675
gwascentralrs730881675
openSNPrs730881675
23andMers730881675
23andMe allrs730881675
SNP Nexus

SNPshotrs730881675
SNPdbers730881675
MSV3drs730881675
GWAS Ctlgrs730881675
Max Magnitude0
ClinVar
Risk rs730881675(;)
Alt rs730881675(;)
Reference rs730881675(ACCCGTGCACGACG;ACCCGTGCACGACG)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene CDKN2A
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000009.11:g.21971105_21971118delCGTCGTGCACGGGT
CLNSRC
CLNACC RCV000160406.1,