Variant (rsID / SNP)

rs2303262

rs2303262 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MPHOSPH6. Location: chromosome 16, position 82,203,758. The table records no clinical significance for this variant.

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Reference-table entries

MPHOSPH6Not classified

Variant type: missense_variant
Chromosome / position: 16:82203758
HGVS: NM_005792.2,c.23G>A,p.Arg8Lys
Allele change: Missense_R8K

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.