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Variant (rsID / SNP)

rs961360

R3HDM1

rs961360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HDM1. Location: chromosome 2, position 136,393,658. The table records no clinical significance for this variant.

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Reference-table entries

R3HDM1Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
2:136393658
HGVS
NM_001378107.1,c.808A>G,p.Met270Val
Allele change
Missense_M226V

Associated conditions / phenotypes

Missense_M270V

Public references

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