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Variant (rsID / SNP)

rs2273962

NCR2

rs2273962 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCR2. Location: chromosome 6, position 41,318,438. The table records no clinical significance for this variant.

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Reference-table entries

NCR2Not classified
Variant type
missense_variant
Chromosome / position
6:41318438
HGVS
NM_004828.4,c.667A>G,p.Met223Val
Allele change
Missense_M223V

Public references

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