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Variant (rsID / SNP)

rs12449313

SMCR8

rs12449313 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SMCR8. Location: chromosome 17, position 18,221,010. The table records no clinical significance for this variant.

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Reference-table entries

SMCR8Not classified
Variant type
missense_variant
Chromosome / position
17:18221010
HGVS
NM_144775.3,c.1907A>G,p.Asn636Ser
Allele change
Missense_N636S

Public references

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