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Variant (rsID / SNP)

rs2305165

R3HDM1

rs2305165 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HDM1. Location: chromosome 2, position 136,409,574. The table records no clinical significance for this variant.

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Reference-table entries

R3HDM1Not classified
Variant type
missense_variant
Chromosome / position
2:136409574
HGVS
NM_001378107.1,c.2000A>C,p.Gln667Pro
Allele change
Missense_Q504P

Associated conditions / phenotypes

Missense_Q633P

Public references

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