Variant (rsID / SNP)

rs1801270

rs1801270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CDKN1A. Location: chromosome 6, position 36,651,971. Clinical significance in the table: Benign.

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Reference-table entries

CDKN1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:36651971
Cytoband: 6p21.2
HGVS: NM_000389.5(CDKN1A):c.93C>A (p.Ser31Arg)
Allele change: Missense_S31R

Associated conditions / phenotypes

CIP1/WAF1 TUMOR-ASSOCIATED POLYMORPHISM 1

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.