Variant (rsID / SNP)

rs55637216

rs55637216 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEMA7A. Location: chromosome 15, position 74,709,717. Clinical significance in the table: Affects.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SEMA7AOther

Clinical significance (as recorded): Affects
Variant type: single nucleotide variant
Chromosome / position: 15:74709717
Cytoband: 15q24.1
HGVS: NM_003612.5(SEMA7A):c.620G>A (p.Arg207Gln)
Allele change: Missense_R193Q

Associated conditions / phenotypes

John Milton Hagen blood group system

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.