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Variant (rsID / SNP)

rs1563632

SMCR8

rs1563632 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMCR8. Location: chromosome 17, position 18,220,770. The table records no clinical significance for this variant.

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Reference-table entries

SMCR8Not classified
Variant type
missense_variant
Chromosome / position
17:18220770
HGVS
NM_144775.3,c.1667G>A,p.Arg556His
Allele change
Missense_R556H

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.