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Variant (rsID / SNP)

rs2072374

NCAPD2

rs2072374 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NCAPD2. Location: chromosome 12, position 6,637,845. The table records no clinical significance for this variant.

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Reference-table entries

NCAPD2Not classified
Variant type
splice_region_variant&synonymous_variant
Chromosome / position
12:6637845
HGVS
NM_014865.4,c.3300T>C,p.Arg1100Arg
Allele change
Synonymous_R1100R

Public references

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