Variant (rsID / SNP)

rs6136

rs6136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SELP. Location: chromosome 1, position 169,563,951. Clinical significance in the table: Benign.

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Reference-table entries

SELPBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:169563951
Cytoband: 1q24.2
HGVS: NM_003005.4(SELP):c.2266A>C (p.Thr756Pro)
Allele change: Missense_T756P

Associated conditions / phenotypes

SELECTIN P POLYMORPHISM

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.