Variant (rsID / SNP)

rs2877380

rs2877380 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CBR4. Location: chromosome 4, position 169,928,842. The table records no clinical significance for this variant.

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Reference-table entries

CBR4Not classified

Variant type: missense_variant
Chromosome / position: 4:169928842
HGVS: NM_032783.5,c.208C>A,p.Leu70Met
Allele change: Missense_L70M

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.