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Variant (rsID / SNP)

rs7193541

RFWD3

rs7193541 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RFWD3. Location: chromosome 16, position 74,664,743. The table records no clinical significance for this variant.

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Reference-table entries

RFWD3Not classified
Variant type
missense_variant
Chromosome / position
16:74664743
HGVS
NM_001370534.1,c.1690A>G,p.Ile564Val
Allele change
Missense_I564V

Associated conditions / phenotypes

Lung Cancer Susceptibility 1|Myeloma, Multiple|Lung Cancer

Public references

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