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Variant (rsID / SNP)

rs3744741

GEMIN4

rs3744741 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GEMIN4. Location: chromosome 17, position 649,232. The table records no clinical significance for this variant.

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Reference-table entries

GEMIN4Not classified
Variant type
missense_variant
Chromosome / position
17:649232
HGVS
NM_015721.3,c.2051G>A,p.Arg684Gln
Allele change
Missense_R684Q

Associated conditions / phenotypes

Disease by Infectious Agent|Lymphoma|Mycobacterium Tuberculosis 1|Renal Cell Carcinoma, Nonpapillary

Public references

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