Variant (rsID / SNP)

rs4971007

rs4971007 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SEMA6C. Location: chromosome 1, position 151,108,137. The table records no clinical significance for this variant.

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Reference-table entries

SEMA6CNot classified

Variant type: missense_variant
Chromosome / position: 1:151108137
HGVS: NM_001178061.3,c.1363A>C,p.Thr455Pro
Allele change: Missense_T455P

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.