rs28939377

Merged into

rs119478058

Orientation

plus

Stabilized

plus

Make rs28939377(C;C)

Make rs28939377(C;T)

Make rs28939377(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

102923789

Gene

AMN

is a	snp
is	mentioned by
dbSNP	rs28939377
dbSNP (classic)	rs28939377
ClinGen	rs28939377
ebi	rs28939377
HLI	rs28939377
Exac	rs28939377
Gnomad	rs28939377
Varsome	rs28939377
LitVar	rs28939377
Map	rs28939377
PheGenI	rs28939377
Biobank	rs28939377
1000 genomes	rs28939377
hgdp	rs28939377
ensembl	rs28939377
geneview	rs28939377
scholar	rs28939377
google	rs28939377
pharmgkb	rs28939377
gwascentral	rs28939377
openSNP	rs28939377
23andMe	rs28939377
SNPshot	rs28939377
SNPdbe	rs28939377
MSV3d	rs28939377
GWAS Ctlg	rs28939377

Status

Merged into rs119478058

Max Magnitude

0

OMIM	605799
Desc	MEGALOBLASTIC ANEMIA 1, NORWEGIAN TYPE
Variant	0002
Related	also