Variant (rsID / SNP)

rs2251555

rs2251555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BEND7. Location: chromosome 10, position 13,534,851. The table records no clinical significance for this variant.

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Reference-table entries

BEND7Not classified

Variant type: synonymous_variant
Chromosome / position: 10:13534851
HGVS: NM_152751.3,c.441T>C,p.Pro147Pro
Allele change: Synonymous_P147P

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.