Variant (rsID / SNP)

rs1062633

rs1062633 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MST1R. Location: chromosome 3, position 49,924,940. The table records no clinical significance for this variant.

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Reference-table entries

MST1RNot classified

Variant type: missense_variant
Chromosome / position: 3:49924940
HGVS: NM_002447.4,c.4003A>G,p.Arg1335Gly
Allele change: Missense_R1229G

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.